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    Company profile for Pfizer Inc

    Gentec Pharmaceutical Group is focused on manufacturing & developing APIs/HPAPIs, Advanced Intermediates & Fine Chemicals.

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    Smithfield BioScience transforms bioproducts into trusted, life-saving therapies through safe, reliable U.S.-based manufacturing.

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    Evonik

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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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    Temad- We think of world-class quality.

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    About

    At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products. Our global portfolio includes medicines and vaccines as well as many of the world's best-known consumer health care products. Every day, Pfizer colleagues work across...
    At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products. Our global portfolio includes medicines and vaccines as well as many of the world's best-known consumer health care products. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Consistent with our responsibility as one of the world's premier innovative bioph

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    Pfizer IncUnited_States_of_America Flag
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    235 East 42nd Street New York, NY 10017
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    INTERVIEW #SpeakPharma

    [Sponsored by another company]
    "50 Years of Innovation: Mikart

    mic"50 Years of Innovation: Mikart's legacy and what's next in CDMO excellence"

    This week, SpeakPharma interviews Michael Kallelis, CEO of Mikart, a leading contract development and manufacturing organization (CDMO) celebrating its 50th anniversary in the pharmaceutical industry. Based in the United States, Mikart has built a reputation for technical expertise, flexible business terms, and specialized capabilities in pharmaceutical development services. In this exclusive interview, Kallelis discusses how Mikart maintains its competitive edge through its Pharmaceutical Development Services team, quality control framework, and commitment to customized business solutions. Kallelis also explores the company's focus on liquid suspensions manufacturing, driven by growing demand from aging populations and pediatric patients, and explains how Mikart balances traditional family business values with modern innovation. HIGHLIGHTS// celebrating its 50th anniversary/ reputation for technical expertise/ how Mikart maintains its competitive edge Mikart is celebrating 50 years in business this year — what are some of the major milestones that have shaped the company's journey? Over our 50-year history, we've celebrated many memorable milestones, but one of the most significant in recent years has been achieving our growth objectives. This success was driven by the strategic expansion of our Pharmaceutical Development Services team, the completion of full aggregate serialization in our packaging department, modernization of our IT systems, enhanced productivity, and our ability to attract both new and returning customers. HIGHLIGHTS// expansion of our Pharmaceutical Development Services team/ completion of full aggregate serialization/ attract both new and returning customers How has Mikart maintained its competitive edge in a constantly evolving pharmaceutical landscape? Our customers consistently tell us that what sets us apart is our technical expertise, high service level, and flexible, customized business terms. At the core of our competitiveness is our focus on Pharmaceutical Development Services (PDS). Mikart's PDS opinion leaders are actively engaged in business development and form early, collaborative relationships with our customers' technical teams. From the outset, our prospects and clients work directly with Mikart's experienced formulation chemists, analytical method developers, and process-oriented engineers to design robust, reproducible, and efficient processes. This hands-on development approach is supported by a comprehensive quality control testing framework — covering raw material testing, in-process checks, on-site microbiological testing, and in-house stability studies. Oversight is provided by our robust Quality Management System, managed by a dedicated Quality Assurance and Regulatory Affairs team. The result is disciplined problem-solving, timely FDA submissions, and a "right-first-time" philosophy that accelerates time-to-market. We operate with a strong sense of urgency and consistently deliver a high level of customer satisfaction. What truly differentiates Mikart is our commitment to customized business terms that eliminate common roadblocks seen with other CDMOs. Our secret sauce is our exceptional service and flexibility in helping our customers bring innovative medicines to patients. HIGHLIGHTS// technical expertise, high service level/ flexible, customized business terms/ comprehensive quality control testing framework/ dedicated Quality Assurance and Regulatory Affairs team/ timely FDA submissions/ accelerates time-to-market What capabilities or services does Mikart offer today that didn't exist 10 or 20 years ago? Mikart was an early leader in serialization, implementing full capabilities well ahead of the industry timeline. This proactive approach has kept our packaging team in high demand. We also upgraded our tablet compression equipment to enhance both speed and reliability. To support growing development needs, we invested in new lab-scale development equipment, unit dose cup filling, sachet packaging, low-humidity suites, and a brand-new suite dedicated to closed-system manufacturing of liquids and suspensions. Most recently, we launched a multi-million dollar expansion of our packaging lines to support higher-speed tablet filling, powder-in-bottle formats, and new liquid fill capabilities. HIGHLIGHTS// early leader in serialization/ upgraded our tablet compression equipment/ multi-million dollar expansion of our packaging lines Why are liquid suspensions becoming such a key focus, and how is Mikart positioned? Formulating suspensions is a complex process that requires specialized expertise and equipment. According to our customers, few mid-market CDMOs do it well — and Mikart is one of them. There is growing industry demand for high-quality suspension manufacturing, driven by the needs of the aging baby boomer population and pediatric patients. For both groups, swallowing tablets or capsules can be difficult, making oral liquid suspensions a more practical alternative. In addition to being easier to administer, suspensions offer pharmacological advantages and can improve dosing compliance. Enhanced flavoring techniques further improve the patient experience — especially for children and infants — by making medicines more palatable. HIGHLIGHTS// growing industry demand for high-quality suspension manufacturing/ suspensions offer pharmacological advantages/ improve dosing compliance How does Mikart balance tradition with innovation to meet modern customer demands? At Mikart, we work hard to preserve the values of a traditional family business, even as we continue to modernize. Our goal is to make every customer feel like they are our top priority. Each customer is supported by a dedicated project manager who serves as their primary point of contact, along with direct access to key team members across departments. This structure ensures our customers are never isolated from our subject matter experts and can get timely, accurate answers to their questions. We're also mindful of the "technology trap" — the tendency to pursue every new innovation at the expense of focus and efficiency. Instead, we rely on market data and customer trends to guide our investments, enabling us to concentrate our resources and capital on technologies that meet real market needs. HIGHLIGHTS// customer is supported by a dedicated project manager/ customers are never isolated from our subject matter experts/ we rely on market data and customer trends to guide our investments/ meet real market needs Looking ahead, what's in store for Mikart in the next 5-10 years? Mikart's strategic plan is now in full motion, and with the momentum we've built, 50 percent growth is within reach. This projection is backed by a strong pipeline of annual FDA filings, a growing customer base, and a robust portfolio of active Pharmaceutical Development Services projects. As we grow, we remain committed to delivering exceptional service and continuously evolving to meet the changing needs of our customers. With renewed political emphasis on domestic manufacturing for the US market, we are ideally positioned to support the rapid, cost-effective development and production of high-quality medicines here at home. As we approach our 50th anniversary in the CDMO industry, we celebrate our legacy and look forward with optimism to the opportunities ahead in the next 5 to 10 years. HIGHLIGHTS// 50 percent growth is within reach/ strong pipeline of annual FDA filings 

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    https://www.pharmacompass.com/speak-pharma/50-years-of-innovation-mikart-s-legacy-and-what-s-next-in-cdmo-excellence

    PharmaCompass
    17 Jul 2025
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    VLOG #PharmaReel

    [Sponsored by another company]

    ReelPharmaQuality, Reliability, TrustQuality, Reliability, Trust

    Quality, Reliability, Trust
    Quality, Reliability, Trust

    reelQuality, Reliability, Trust

    This PharmaReel highlights Rochem’s capabilities in sourcing and supplying Generic APIs and Excipients, driven by Quality, Reliability, and Trust through fully cGMP-compliant operations. With over 30 years of experience and 16 offices worldwide, Rochem continues to develop partnerships across the US, China, Europe, and South America.

    Impressions: 3300

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    DATA COMPILATION #PharmaFlow

    [Sponsored by another company]
    CDMO Activity Tracker: Veranova, Carbogen lead ADC investments; Axplora, Polfa Tarchomin, Famar expand European footprint

    CDMO Activity Tracker: Veranova, Carbogen lead ADC investments; Axplora, Polfa Tarchomin, Famar expand European footprint

    During the second quarter (Q2) of 2025, contract development and manufacturing organizations (CDMOs) made substantial investments in specialized therapeutic manufacturing. The quarter also saw CDMOs pursue high-value, complex manufacturing niches, particularly in antibody-drug conjugates (ADCs), cell and gene therapies (CGTs) and oligonucleotides.Alongside these trends, Q2 also saw CDMOs strengthen their footprint in the United States amid concerns over rising tariffs and unpredictable trade policies being enforced by the Trump administration.Regeneron Pharmaceuticals committed over US$ 3 billion through a 10-year agreement with Fujifilm Diosynth Biotechnologies to nearly double its US manufacturing capacity for biologics. Under this agreement, Fujifilm will manufacture and supply drug products for Regeneron at its large-scale facility in Holly Springs, North Carolina.Thermo Fisher Scientific announced plans to invest an additional US$ 2 billion in the US over four years, reinforcing its manufacturing and R&D capabilities. With 64 facilities spread across 37 states, Thermo Fisher aims to bolster American innovation and competitiveness. Similarly, Piramal Pharma announced a US$ 90 million investment plan for expanding two facilities in the US, thereby bringing its total investment in the country to US$ 570 million. View CDMO Activity Tracker for Q2 2025 (Free Excel Available)Veranova, Carbogen lead ADC wave; Axplora doubles down on HPAPI production in ItalyThe quarter saw substantial investments in ADC manufacturing. Veranova announced a US$ 20 million investment in bioconjugation development and cGMP manufacturing capacity at its Devens, Massachusetts campus. With this investment, Veranova will be able to provide a more comprehensive suite of services to its partners developing ADCs and other bioconjugates. Veranova’s total investment in the Devens facility now stands at over US$ 50 million. Swiss CDMO Carbogen announced a US$ 31 million co-investment with an unnamed Japanese investor to expand its capabilities across its Aarau and Neuland (Switzerland) facilities. The facility will address increasing demand for complex and high-value compounds such as ADC drug linkers.Axplora announced a further €35 million (US$ 41 million) expansion of its Farmabios site in Italy, doubling the facility to approximately 108,000 square meters by mid-2026. This investment raises its total spend on the site to over €80 million (US$ 94.05 million) since 2019, supporting the production of highly potent active pharmaceutical ingredients (HPAPIs). Farmabios now stands as a key hub in Axplora’s global CDMO network.Polish pharmaceutical manufacturer Polfa Tarchomin is positioning itself as a significant player in the European CDMO market through its investment in the Center for Development and Production of Highly Potent Drugs. This 12,000 square meter facility has two state-of-the-art production lines designed for filling vials and pre-filled syringes with an annual capacity of 26 million product units.Skyepharma’s projected annual revenues from oncology-linked activities touched €10 million (US$ 11.2 million). The CDMO’s facility in Saint-Quentin-Fallavier is equipped to handle cytotoxic and cytostatic compounds, and is one of the few facilities in France capable of managing HPAPIs for oral anticancer treatments. View CDMO Activity Tracker for Q2 2025 (Free Excel Available) Athena acquires Medipha Santé, Famar buys MiP Pharma’s German site to strengthen European footprintDuring the quarter, several CDMOs enhanced their strategic capabilities through M&As. Athena Pharmaceutiques acquired  Medipha Santé to build a fully integrated pharmaceutical services platform in Europe. Based in Paris, Athena has strengthened its commercial and regulatory toolbox by bringing aboard Medipha Santé’s 35-strong team, which supports over 100 partner organizations and files approximately 350 dossiers annually with ANSM and other European agencies. With this integration, Athena positions itself as a one-stop CDMO partner.With the acquisition of MiP Pharma’s sterile manufacturing site in Homburg, Germany, the Famar Group has expanded its capabilities in aseptic and lyophilized fill-and-finish operations. The acquisition has strengthened Famar’s position in sterile drug manufacturing. The CDMO now has seven manufacturing facilities in Europe.PCI Pharma Services’ acquisition of Ajinomoto Althea has established a world-class, large-scale manufacturing hub in the San Diego region with state-of-the-art aseptic facilities for prefilled syringes, cartridges and high-potent formulations such as ADCs. PCI Pharma is now amongst the few US-based CDMOs capable of comprehensive ADC manufacturing.Samsung Biologics’ strategic spinoff of its biosimilar business stood out as a significant corporate restructuring exercise during the quarter. The separation of Samsung Bioepis, tentatively renamed Samsung Epis Holdings, aims to enhance Samsung Biologics’ strategic focus and build client trust, as it eliminates potential conflicts between CDMO services and proprietary drug development. The move came after Samsung Biologics inked a contract worth 737.3 billion Korean won (US$ 518 million) with an undisclosed US pharmaceutical company.WuXi Biologics announced a US$ 167 million divestment of its German facility to Terumo and broke ground on a microbial production plant in China. National Resilience, which was launched five years ago as the US drug manufacturer dedicated to broadening access to medicines and protecting biopharma supply chains, said it is shuttering six of its 10 facilities. The company said the sites were “not being fully utilized.” View CDMO Activity Tracker for Q2 2025 (Free Excel Available) MilliporeSigma, Simtra form 5-year ADC alliance; Silexion partners Catalent for siRNA developmentMerck KGaA’s MilliporeSigma and Simtra struck a five-year strategic alliance, combining expertise across the ADC value chain to reduce development timelines and complexity for biopharmaceutical companies. Viralgen collaborated with Trogenix to rapidly scale product supply for TGX-007, an AAV gene therapy for glioblastoma (a type of cancer of the brain and spinal cord).  Silexion announced a collaboration with Catalent for small interfacing RNA (siRNA) development and manufacturing. Catalent’s Limoges (France) facility will conduct formulation development and clinical manufacturing for Silexion’s SIL204 candidate, supporting both systemic and intra-tumoral delivery formulations.Skyepharma’s collaboration with Eneapharm through the Skyehub platform aims to support the treatment of patients suffering from exocrine pancreatic insufficiency, including those affected by cystic fibrosis or pancreatic cancer. Orion Corporation reached an agreement with Shilpa Biocare for the distribution of recombinant human albumin in Europe.Meanwhile, Aenova announced the launch of its Aenovation program, an initiative designed to fast-track early development of pharmaceutical formulations. The program addresses the critical challenges of bioavailability and time-to-market faced by poorly soluble drug candidates. View CDMO Activity Tracker for Q2 2025 (Free Excel Available) Our view The quarter saw CDMO developments mimic the broader trends in the pharmaceutical industry, such as onshoring of critical manufacturing capabilities in the US, consolidation of specialized expertise through strategic partnerships, and the relentless focus on emerging therapeutic modalities that promise to transform patient care. With CDMOs continuing to invest in next-generation manufacturing capabilities, we expect the sector to play a crucial role in drug innovation. 
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    Impressions: 7375

    https://www.pharmacompass.com/radio-compass-blog/cdmo-activity-tracker-veranova-carbogen-lead-adc-investments-axplora-polfa-tarchomin-famar-expand-european-footprint

    #PharmaFlow by PHARMACOMPASS
    10 Jul 2025
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    NEWS #PharmaBuzz

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    Pfizer's Sickle-Cell Treatment Effort Falter as Drug Fails Study
    Pfizer's Sickle-Cell Treatment Effort Falter as Drug Fails Study

    18 Aug 2025

    // REUTERS

    https://www.reuters.com/business/healthcare-pharmaceuticals/pfizers-sickle-cell-treatment-efforts-falter-drug-fails-study-2025-08-15/

    REUTERS
    18 Aug 2025
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    Padcev-Keytruda Combo Delivers Bladder Cancer 'breakthrough'
    Padcev-Keytruda Combo Delivers Bladder Cancer 'breakthrough'

    13 Aug 2025

    // PRESS RELEASE

    https://www.pfizer.com/news/press-release/press-release-detail/padcevtm-plus-keytrudatm-significantly-improves-survival

    PRESS RELEASE
    13 Aug 2025
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    FDA May Reject Renewal of Pfizer's Kid COVID Shot Authorization
    FDA May Reject Renewal of Pfizer's Kid COVID Shot Authorization

    12 Aug 2025

    // FIERCE PHARMA

    https://www.fiercepharma.com/pharma/fda-may-not-renew-pfizers-pediatric-covid-shot-authorization-prompting-potential

    FIERCE PHARMA
    12 Aug 2025
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    Pfizer Debuts 20-Valent Pneumococcal Vaccine for Adults in India
    Pfizer Debuts 20-Valent Pneumococcal Vaccine for Adults in India

    12 Aug 2025

    // INDPHARMAPOST

    https://www.indianpharmapost.com/news/pfizer-launches-20-valent-pneumococcal-conjugate-vaccine-for-adults-in-india-17583

    INDPHARMAPOST
    12 Aug 2025
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    CureVac Settles mRNA Patent Dispute with Pfizer & Biontech
    CureVac Settles mRNA Patent Dispute with Pfizer & Biontech

    09 Aug 2025

    // REUTERS

    https://www.reuters.com/business/healthcare-pharmaceuticals/curevac-settles-mrna-patent-dispute-litigation-with-pfizer-biontech-2025-08-08/

    REUTERS
    09 Aug 2025
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    Pfizer Completes Licensing Agreement with 3SBio
    Pfizer Completes Licensing Agreement with 3SBio

    26 Jul 2025

    // PRESS RELEASE

    https://www.pfizer.com/news/press-release/press-release-detail/pfizer-completes-licensing-agreement-3sbio

    PRESS RELEASE
    26 Jul 2025
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    ALL APIs

    read-moreClick the button for full data set
    read-moreClick the button for full data set

    01

    Betamethyl Epoxide

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    ACS Fall 2025
    Not Confirmed
    arrow

    Betamethyl Epoxide

    U.S.A

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    USDMF arrow-down Click Us! arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 11848

    Submission : 1996-02-08

    Status : Active

    Type : II

     CEP/COS Inactive-api
    ✖

    Certificate Number : R0-CEP 2001-070 - Rev 00

    Issue Date : 2002-03-04

    Type : TSE

    Substance Number :

    Status : Expired

     JDMF arrow-down
    ✖

    Registration Number : 222MF10213

    Registrant's Address : 7000 Portage Road, Kalamazoo, Michigan 49001, USA

    Initial Date of Registration : 2010-08-05

    Latest Date of Registration :

    EU-WC NDC KDMF VMF Others AUDIT
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    02

    Epoprostenol Sodium

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    ACS Fall 2025
    Not Confirmed
    arrow

    Epoprostenol Sodium

    U.S.A

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 6065

    Submission : 1985-10-16

    Status : Active

    Type : II

     CEP/COS JDMF arrow-down
    ✖

    Registration Number : 218MF10929

    Registrant's Address : 7000 Portage Road, Kalamazoo, Michigan 49001, USA

    Initial Date of Registration : 2006-11-21

    Latest Date of Registration :

    EU-WC NDC arrow-down
    ✖

    NDC Package Code : 0009-5164

    Start Marketing Date : 2014-07-03

    End Marketing Date : 2025-12-31

    Dosage Form (Strength) : POWDER (1g/g)

    Marketing Category : BULK INGREDIENT

    KDMF VMF Others AUDIT
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    #PipelineProspector

    Market
    Place

    03

    Methylprednisolone

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    ACS Fall 2025
    Not Confirmed
    arrow

    Methylprednisolone

    U.S.A

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 4796

    Submission : 1983-01-06

    Status : Active

    Type : II

     CEP/COS arrow-down
    ✖

    Certificate Number : CEP 2006-058 - Rev 03

    Issue Date : 2024-03-07

    Type : Chemical

    Substance Number : 561

    Status : Valid

     JDMF EU-WC NDC arrow-down
    ✖

    NDC Package Code : 0009-0038

    Start Marketing Date : 2014-07-03

    End Marketing Date : 2025-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

    KDMF VMF Others AUDIT
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    #PipelineProspector

    Market
    Place

    04

    Prednisolone

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    ACS Fall 2025
    Not Confirmed
    arrow

    Prednisolone

    U.S.A

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    USDMF Inactive-api
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 1432

    Submission : 1969-09-18

    Status : Inactive

    Type : II

     CEP/COS Inactive-api
    ✖

    Certificate Number : R0-CEP 2001-018 - Rev 00

    Issue Date : 2001-10-24

    Type : TSE

    Substance Number :

    Status : Withdrawn by Holder

     JDMF arrow-down
    ✖

    Registration Number : 227MF10238

    Registrant's Address : 7000 Portage Road, Kalamazoo, Michigan 49001, USA

    Initial Date of Registration : 2015-09-29

    Latest Date of Registration :

    EU-WC NDC KDMF VMF Others AUDIT
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    05

    Dexamethasone

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    ACS Fall 2025
    Not Confirmed
    arrow

    Dexamethasone

    U.S.A

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    USDMF CEP/COS Inactive-api
    ✖

    Certificate Number : R0-CEP 2001-046 - Rev 00

    Issue Date : 2002-01-28

    Type : TSE

    Substance Number :

    Status : Expired

     JDMF arrow-down
    ✖

    Registration Number : 221MF10091

    Registrant's Address : 7000 Portage Road, Kalamazoo, Michigan 49001, USA

    Initial Date of Registration : 2009-05-13

    Latest Date of Registration :

    EU-WC NDC arrow-down
    ✖

    NDC Package Code : 0009-5010

    Start Marketing Date : 2016-05-18

    End Marketing Date : 2025-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

    KDMF arrow-down
    ✖

    Registrant Name : Novartis Korea Ltd.

    Registration Date : 2022-11-02

    Registration Number : 20220422-209-J-1258(1)

    Manufacturer Name : Pharmacia & Upjohn Company LLC

    Manufacturer Address : 7000 Portage Road, Kalamazoo, Michigan 49001, USA

     VMF Others AUDIT
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    06

    Estradiol Cypionate

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    ACS Fall 2025
    Not Confirmed
    arrow

    Estradiol Cypionate

    U.S.A

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 5047

    Submission : 1983-07-25

    Status : Active

    Type : II

     CEP/COS Inactive-api
    ✖

    Certificate Number : R0-CEP 2000-394 - Rev 00

    Issue Date : 2001-11-05

    Type : TSE

    Substance Number :

    Status : Withdrawn by Holder

     JDMF EU-WC NDC KDMF VMF Others AUDIT
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    #PipelineProspector

    Market
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    07

    Estramustine Sodium Phosphate

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    ACS Fall 2025
    Not Confirmed
    arrow

    Estramustine Sodium Phosphate

    U.S.A

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    ACS Fall 2025
    Not Confirmed
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    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 6258

    Submission : 1986-03-27

    Status : Active

    Type : II

     CEP/COS Inactive-api
    ✖

    Certificate Number : R0-CEP 2000-408 - Rev 00

    Issue Date : 2001-11-16

    Type : TSE

    Substance Number :

    Status : Withdrawn by Holder

     JDMF EU-WC NDC KDMF VMF Others AUDIT
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    08

    Methylprednisolone Acetate

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    ACS Fall 2025
    Not Confirmed
    arrow

    Methylprednisolone Acetate

    U.S.A

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 4813

    Submission : 1983-01-06

    Status : Active

    Type : II

     CEP/COS Inactive-api
    ✖

    Certificate Number : R0-CEP 2000-363 - Rev 00

    Issue Date : 2001-10-24

    Type : TSE

    Substance Number : 933

    Status : Withdrawn by Holder

     JDMF EU-WC NDC arrow-down
    ✖

    NDC Package Code : 0009-0026

    Start Marketing Date : 2014-07-03

    End Marketing Date : 2025-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

    KDMF VMF Others AUDIT
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    Market
    Place

    09

    Clindamycin Palmitate

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    ACS Fall 2025
    Not Confirmed
    arrow

    Clindamycin Palmitate

    U.S.A

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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    ACS Fall 2025
    Not Confirmed
    • fda
    • EDQM
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    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : Reviewed

    Rev. Date : 2015-01-29

    Pay. Date : 2015-01-26

    DMF Number : 13412

    Submission : 1998-09-01

    Status : Active

    Type : II

     CEP/COS JDMF EU-WC NDC arrow-down
    ✖

    NDC Package Code : 0009-0063

    Start Marketing Date : 2014-07-03

    End Marketing Date : 2025-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

    KDMF VMF Others AUDIT
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    Market
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    10

    Clindamycin Phosphate

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    ACS Fall 2025
    Not Confirmed
    arrow

    Clindamycin Phosphate

    U.S.A

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
    • EDQM
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    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 13413

    Submission : 1998-09-01

    Status : Active

    Type : II

     CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
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    USDMF

    read-more
    read-more

    01

    10-deacetyl Baccatin Iii

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    02

    17a-methyltestosterone

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    03

    5-ethyl-2"-deoxyuridine

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    04

    8-arginine Vasopressin (8-avp)

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    05

    9-aminocamptothecin Active Drug Subs...

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    06

    9-aminocamptothecin Colloidal Disper...

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    07

    Achromycin (tetracycline) Bulk

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    08

    Activated Calicheamicin Derivative

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    09

    Amphotericin B

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    10

    Ampicillin Sodium

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow
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    CEP/COS

    read-more
    read-more

    01

    16-alpha-Hydroxyprednisolone

    CEP/COS

    ACS Fall 2025
    Not Confirmed
    arrow

    02

    3-oxo-4-azaandrost-5-ene-17beta-carboxyl...

    CEP/COS

    ACS Fall 2025
    Not Confirmed
    arrow

    03

    Alphamethyl Epoxide

    CEP/COS

    ACS Fall 2025
    Not Confirmed
    arrow

    04

    Alprazolam, Milled/micronised

    CEP/COS

    ACS Fall 2025
    Not Confirmed
    arrow

    05

    Betamethasone Triene, (Betamethasone 6/6...

    CEP/COS

    ACS Fall 2025
    Not Confirmed
    arrow

    06

    Betamethasone valerate

    CEP/COS

    ACS Fall 2025
    Not Confirmed
    arrow

    07

    Betamethyl Epoxide, 11 DB, (17a,21-dihyd...

    CEP/COS

    ACS Fall 2025
    Not Confirmed
    arrow

    08

    Cabergoline

    CEP/COS

    ACS Fall 2025
    Not Confirmed
    arrow

    09

    Carboplatin

    CEP/COS

    ACS Fall 2025
    Not Confirmed
    arrow

    10

    Cisplatin

    CEP/COS

    ACS Fall 2025
    Not Confirmed
    arrow
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    JDMF

    read-more
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    01

    16α - hydroxy prednisolone

    JDMF

    ACS Fall 2025
    Not Confirmed
    arrow

    16α - hydroxy prednisolone

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
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    Pfizer Inc

    Registration Number : 227MF10238

    Registrant's Address : 7000 Portage Road, Kalamazoo, Michigan 49001, USA

    Initial Date of Registration : 2015-09-29

    Latest Date of Registration : 2015-09-29

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    Market
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    02

    Betamethyl Epoxide

    JDMF

    ACS Fall 2025
    Not Confirmed
    arrow

    Betamethyl Epoxide

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
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    • WHO-GMP
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    Pfizer Inc

    Registration Number : 222MF10213

    Registrant's Address : 7000 Portage Road, Kalamazoo, Michigan 49001, USA

    Initial Date of Registration : 2010-08-05

    Latest Date of Registration : 2010-08-05

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    03

    Chlormadinone Acetate

    JDMF

    ACS Fall 2025
    Not Confirmed
    arrow

    Chlormadinone Acetate

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
    • EDQM
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    Pfizer Inc

    Registration Number : 217MF10977

    Registrant's Address : 235 East 42nd Street, New York, NY 10017

    Initial Date of Registration : 2005-11-14

    Latest Date of Registration : 2009-05-27

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    Market
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    04

    Dexamethasone

    JDMF

    ACS Fall 2025
    Not Confirmed
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    Dexamethasone

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Pfizer Inc

    Registration Number : 221MF10091

    Registrant's Address : 7000 Portage Road, Kalamazoo, Michigan 49001, USA

    Initial Date of Registration : 2009-05-13

    Latest Date of Registration : 2010-05-31

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    Market
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    05

    Epoprostenol sodium

    JDMF

    ACS Fall 2025
    Not Confirmed
    arrow

    Epoprostenol sodium

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Pfizer Inc

    Registration Number : 218MF10929

    Registrant's Address : 7000 Portage Road, Kalamazoo, Michigan 49001, USA

    Initial Date of Registration : 2006-11-21

    Latest Date of Registration : 2006-11-21

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    Market
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    06

    Progesterone

    JDMF

    ACS Fall 2025
    Not Confirmed
    arrow

    Progesterone

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Pfizer Inc

    Registration Number : 225MF10081

    Registrant's Address : 7000 Portage Road, Kalamazoo, Michigan 49001, USA

    Initial Date of Registration : 2013-04-18

    Latest Date of Registration : 2013-04-18

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    Market
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    07

    CRM197

    JDMF

    ACS Fall 2025
    Not Confirmed
    arrow

    CRM197

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
    • EDQM
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    Wyeth Pharmaceuticals Inc

    Registration Number : 226MF10009

    Registrant's Address : 66 Hudson Boulevard East New York, NY 10001-2192

    Initial Date of Registration : 2014-01-08

    Latest Date of Registration : 2022-12-23

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    KDMF

    read-more
    read-more

    01

    Abrocitinib

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    Abrocitinib

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Pfizer Inc

    Registrant Name : Korea Pfizer Pharmaceutical Co., Ltd.

    Registration Date : 2021-11-23

    Registration Number : 87-29-ND

    Manufacturer Name : Pfizer Ireland Pharmaceuticals

    Manufacturer Address : Ringaskiddy API Plant Rinaskiddy Country Cork Ireland

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    Market
    Place

    02

    Alprazolam

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    Alprazolam

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Pfizer Inc

    Registrant Name : Beatrice Korea Co., Ltd.

    Registration Date : 2021-03-16

    Registration Number : 20210316-209-J-884

    Manufacturer Name : Pharmacia & Upjohn Company

    Manufacturer Address : 7000 Portage Road, Kalamazoo, Michigan 49001, USA

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    Market
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    03

    Amlodipine besilate

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    Amlodipine besilate

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
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    Pfizer Inc

    Registrant Name : Jeil Pharmaceutical Co., Ltd.

    Registration Date : 2017-06-28

    Registration Number : 20110315-130-H-73-14(1)

    Manufacturer Name : Pfizer Pharmaceuticals LLC

    Manufacturer Address : PO Box 628 KM 58.2 Road No. 2 Barceloneta

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    04

    Amlodipine besilate

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    Amlodipine besilate

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
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    Pfizer Inc

    Registrant Name : Beatrice Korea Co., Ltd.

    Registration Date : 2022-10-24

    Registration Number : 20221024-130-H-403-50

    Manufacturer Name : Pfizer Asia Manufacturing Pte ...

    Manufacturer Address : 31 Tuas South Avenue 6, 637578, Singapore

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    05

    Amlodipine besilate

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    Amlodipine besilate

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
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    Pfizer Inc

    Registrant Name : Beatrice Korea Co., Ltd.

    Registration Date : 2011-03-15

    Registration Number : 20110315-130-H-73-14

    Manufacturer Name : Viatris Pharmaceuticals LLC

    Manufacturer Address : PO Box 628 KM 58.2 Road No. 2 Barceloneta

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    06

    Anidullapunjin

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    Anidullapunjin

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
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    Pfizer Inc

    Registrant Name : Korea Pfizer Pharmaceutical Co., Ltd.

    Registration Date : 2009-11-12

    Registration Number : Su189-11-ND

    Manufacturer Name : Pharmacia & Upjohn Company LLC

    Manufacturer Address : 7000 Portage Road Kalamazoo, Michigan (MI) 49001 United States (USA)

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    07

    Atorvastatin calcium

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    Atorvastatin calcium

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
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    Pfizer Inc

    Registrant Name : HKINNOEN Co., Ltd.

    Registration Date : 2019-09-24

    Registration Number : 20110110-132-H-57-04(1)

    Manufacturer Name : Upjohn Manufacturing Ireland U...

    Manufacturer Address : Little Island, Co, Cork, T45 F627, Ireland

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    08

    Atorvastatin calcium trihydrate

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    Atorvastatin calcium trihydrate

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
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    Pfizer Inc

    Registrant Name : Beatrice Korea Co., Ltd.

    Registration Date : 2016-01-14

    Registration Number : 20160114-132-H-285-34

    Manufacturer Name : Pfizer Ireland Pharmaceuticals

    Manufacturer Address : Ringaskiddy API Plant, PO Box 140, Ringaskiddy, Co. Cork, Ireland

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    09

    Atorvastatin calcium trihydrate

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    Atorvastatin calcium trihydrate

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
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    Pfizer Inc

    Registrant Name : Beatrice Korea Co., Ltd.

    Registration Date : 2011-01-10

    Registration Number : 20110110-132-H-57-04

    Manufacturer Name : Upjohn Manufacturing Ireland U...

    Manufacturer Address : Little Island Co. Cork, T45 F627, Ireland

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    10

    Azithromycin

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    Azithromycin

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
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    Pfizer Inc

    Registrant Name : Korea Pfizer Pharmaceutical Co., Ltd.

    Registration Date : 2020-10-14

    Registration Number : 20201014-191-I-595-07

    Manufacturer Name : Pfizer Asia Manufacturing Pte ...

    Manufacturer Address : 31 Tuas South Avenue 6 Singapore 637578@[erythromycin manufacturing plant ①]1401 Sh...

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    NDC API

    read-more
    read-more

    01

    ALPRAZOLAM

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    ALPRAZOLAM

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
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    Pfizer Inc

    NDC Package Code : 0009-5144

    Start Marketing Date : 2014-07-03

    End Marketing Date : 2025-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

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    02

    ALPROSTADIL

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    ALPROSTADIL

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
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    Pfizer Inc

    NDC Package Code : 0009-0042

    Start Marketing Date : 2015-08-26

    End Marketing Date : 2025-12-31

    Dosage Form (Strength) : POWDER (1g/g)

    Marketing Category : BULK INGREDIENT

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    03

    AMLODIPINE BESYLATE

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    AMLODIPINE BESYLATE

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
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    Pfizer Inc

    NDC Package Code : 68724-0008

    Start Marketing Date : 2020-06-01

    End Marketing Date : 2025-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

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    04

    ANIDULAFUNGIN

    U.S.A
    ACS Fall 2025
    Not Confirmed
    arrow

    ANIDULAFUNGIN

    U.S.A
    arrow
    ACS Fall 2025
    Not Confirmed
    • fda
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    Pfizer Inc

    NDC Package Code : 0009-0043

    Start Marketing Date : 2015-08-26

    End Marketing Date : 2025-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

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    05

    ATORVASTATIN CALCIUM TRIHYDRATE

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    ATORVASTATIN CALCIUM TRIHYDRATE

    U.S.A
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    ACS Fall 2025
    Not Confirmed
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    Pfizer Inc

    NDC Package Code : 61947-0002

    Start Marketing Date : 2011-01-01

    End Marketing Date : 2025-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

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    06

    AZITHROMYCIN DIHYDRATE

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    AZITHROMYCIN DIHYDRATE

    U.S.A
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    ACS Fall 2025
    Not Confirmed
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    Pfizer Inc

    NDC Package Code : 68724-2124

    Start Marketing Date : 2014-07-03

    End Marketing Date : 2025-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

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    07

    AZITHROMYCIN, UNSPECIFIED FORM

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    AZITHROMYCIN, UNSPECIFIED FORM

    U.S.A
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    ACS Fall 2025
    Not Confirmed
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    Pfizer Inc

    NDC Package Code : 60715-3150

    Start Marketing Date : 2011-12-29

    End Marketing Date : 2026-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

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    08

    AZTREONAM

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    AZTREONAM

    U.S.A
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    Hospira, Inc.

    NDC Package Code : 54087-160

    Start Marketing Date : 2012-01-04

    End Marketing Date : 2026-12-31

    Dosage Form (Strength) : POWDER, FOR SOLUTION (75mg/1)

    Marketing Category : DRUG FOR FURTHER PROCESSING

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    09

    BELIMUMAB

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    BELIMUMAB

    U.S.A
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    ACS Fall 2025
    Not Confirmed
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    Hospira, Inc.

    NDC Package Code : 0409-9966

    Start Marketing Date : 2014-03-10

    End Marketing Date : 2025-12-31

    Dosage Form (Strength) : INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION (400mg/5mL)

    Marketing Category : DRUG FOR FURTHER PROCESSING

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    10

    CELECOXIB

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    CELECOXIB

    U.S.A
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    ACS Fall 2025
    Not Confirmed
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    Pfizer Inc

    NDC Package Code : 68724-1004

    Start Marketing Date : 1998-10-02

    End Marketing Date : 2025-12-31

    Dosage Form (Strength) : POWDER (1kg/kg)

    Marketing Category : BULK INGREDIENT

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    Dexamethasone 9,11-Epoxide

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    At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products. Our global portfolio includes medicines and vaccines as well as many of the world's be...
    At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products. Our global portfolio includes medicines and vaccines as well as many of the world's best-known consumer health care products. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Consistent with our responsibility as one of the world's premier innovative bioph
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    01

    Dexamethasone 9,11-Epoxide

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    Dexamethasone 9,11-Epoxide

    U.S.A
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    ACS Fall 2025
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    Pfizer Inc

    At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products. Our global portfolio includes medicines and vaccines as well as many of the world's best-known consumer health care products. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Consistent with our responsibility as one of the world's premier innovative bioph

    About the Company : At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value i...

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    Hydrocortisone Acetate

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    At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products. Our global portfolio includes medicines and vaccines as well as many of the world's be...
    At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products. Our global portfolio includes medicines and vaccines as well as many of the world's best-known consumer health care products. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Consistent with our responsibility as one of the world's premier innovative bioph
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    02

    Hydrocortisone Acetate

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    Hydrocortisone Acetate

    U.S.A
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    ACS Fall 2025
    Not Confirmed
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    Pfizer Inc

    At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products. Our global portfolio includes medicines and vaccines as well as many of the world's best-known consumer health care products. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Consistent with our responsibility as one of the world's premier innovative bioph

    About the Company : At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value i...

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    01

    Brand Name : CIBINQO

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    Brand Name : CIBINQO

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    RLD : Yes

    TE Code :

    ABROCITINIB

    Pfizer Inc

    Dosage Form : TABLET; ORAL

    Proprietary Name : CIBINQO

    Dosage Strength : 50MG

    Approval Date : 2022-01-14

    Application Number : 213871

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    02

    Brand Name : CIBINQO

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    Brand Name : CIBINQO

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    RLD : Yes

    TE Code :

    ABROCITINIB

    Pfizer Inc

    Dosage Form : TABLET; ORAL

    Proprietary Name : CIBINQO

    Dosage Strength : 100MG

    Approval Date : 2022-01-14

    Application Number : 213871

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    03

    Brand Name : CIBINQO

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    Brand Name : CIBINQO

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    RLD : Yes

    TE Code :

    ABROCITINIB

    Pfizer Inc

    Dosage Form : TABLET; ORAL

    Proprietary Name : CIBINQO

    Dosage Strength : 200MG

    Approval Date : 2022-01-14

    Application Number : 213871

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    04

    Brand Name : ACETAZOLAMIDE SODIUM

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    Brand Name : ACETAZOLAMIDE SODIUM

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    RLD : No

    TE Code :

    ACETAZOLAMIDE SODIUM

    Hospira, Inc.

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : ACETAZOLAMIDE SODIUM

    Dosage Strength : EQ 500MG BASE/VIAL

    Approval Date : 1995-10-30

    Application Number : 40108

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    Brand Name : ACETYLCYSTEINE

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    Brand Name : ACETYLCYSTEINE

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    RLD : No

    TE Code :

    ACETYLCYSTEINE

    Hospira, Inc.

    Dosage Form : SOLUTION; INHALATION, ORAL

    Proprietary Name : ACETYLCYSTEINE

    Dosage Strength : 10%

    Approval Date : 1989-05-01

    Application Number : 71364

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    Brand Name : ACETYLCYSTEINE

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    Brand Name : ACETYLCYSTEINE

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    RLD : No

    TE Code :

    ACETYLCYSTEINE

    Hospira, Inc.

    Dosage Form : SOLUTION; INHALATION, ORAL

    Proprietary Name : ACETYLCYSTEINE

    Dosage Strength : 20%

    Approval Date : 1989-05-01

    Application Number : 71365

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    Brand Name : ACETYLCYSTEINE

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    Brand Name : ACETYLCYSTEINE

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    RLD : No

    TE Code : AN

    ACETYLCYSTEINE

    Hospira, Inc.

    Dosage Form : SOLUTION; INHALATION, ORAL

    Proprietary Name : ACETYLCYSTEINE

    Dosage Strength : 10%

    Approval Date : 1994-08-30

    Application Number : 73664

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AN

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    08

    Brand Name : ACETYLCYSTEINE

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    Brand Name : ACETYLCYSTEINE

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    RLD : No

    TE Code : AN

    ACETYLCYSTEINE

    Hospira, Inc.

    Dosage Form : SOLUTION; INHALATION, ORAL

    Proprietary Name : ACETYLCYSTEINE

    Dosage Strength : 20%

    Approval Date : 1994-08-30

    Application Number : 74037

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AN

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    09

    Brand Name : ACYCLOVIR SODIUM

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    Brand Name : ACYCLOVIR SODIUM

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    RLD : No

    TE Code :

    ACYCLOVIR SODIUM

    Hospira, Inc.

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : ACYCLOVIR SODIUM

    Dosage Strength : EQ 500MG BASE/VIAL

    Approval Date : 1997-04-22

    Application Number : 74663

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    Brand Name : ACYCLOVIR SODIUM

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    Brand Name : ACYCLOVIR SODIUM

    U.S.A
    ACS Fall 2025
    Not Confirmed
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    RLD : No

    TE Code :

    ACYCLOVIR SODIUM

    Hospira, Inc.

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : ACYCLOVIR SODIUM

    Dosage Strength : EQ 1GM BASE/VIAL

    Approval Date : 1997-04-22

    Application Number : 74663

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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