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    Company profile for Sun Pharmaceutical Industries Limited

    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    Munit offers scalable GMP micronization and particle size engineering to enhance drug solubility, bioavailability, and performance.

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    Lupin Manufacturing Solutions – delivering high-quality APIs & end-to-end CDMO services for faster, cost-effective drug development.

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    Inke S.A: APIs manufacturing plant.

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    Alchem offers Botanical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.

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    Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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    About

    We were pioneers among Indian pharmaceutical companies to see tremendous value in investing in research & development (R&D). Our early investments in R&D, beginning three decades ago, enabled us to make technology our key differentiator and develop a basket of robust products for diverse markets across the world. Our core strength lies in our ability to excel in developing generics and technologically complex products through ...
    We were pioneers among Indian pharmaceutical companies to see tremendous value in investing in research & development (R&D). Our early investments in R&D, beginning three decades ago, enabled us to make technology our key differentiator and develop a basket of robust products for diverse markets across the world. Our core strength lies in our ability to excel in developing generics and technologically complex products through focused teams in formulations, process chemistry and analytical development. We have the capability to deliver quality products within established timelines, at low costs and without compromising on quality.

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    Sun Pharmaceutical Industries Limitedindia-flag Flag
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    India
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    Sun House, CTS No. 201 B/1, Western Express Highway, Goregaon (E), Mumbai 400...
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    +91-22-4324 4324, +91 22 6696 9696
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    CPhI WW Frankfurt

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    INTERVIEW #SpeakPharma

    [Sponsored by another company]
    “We are building capabilities to stay ahead of the curve, and align with future needs of global healthcare”

    mic“We are building capabilities to stay ahead of the curve, and align with future needs of global healthcare”

    This week, SpeakPharma interviews Girish Chovatia, Chairman and Managing Director of Ami Lifesciences. Since its inception in 2006, Ami Lifesciences has emerged as one of the fastest-growing API manufacturers from India, delivering high-quality active pharmaceutical ingredients (APIs) to global partners across more than 60 countries. With a portfolio of 80+ APIs and strong regulatory accreditations, including those from the US Food and Drug Administration (FDA), European Directorate for the Quality of Medicines & HealthCare (EDQM), and the Pharmaceuticals and Medical Devices Agency (PMDA), the company has built a reputation for innovation, reliability, and customer-centricity.Ami Lifesciences’ ability to combine chemistry expertise with forward-looking strategies such as backward integration, custom synthesis, and a growing focus on platform technologies for next-generation therapeutics sets it apart. The company’s state-of-the-art infrastructure, emphasis on regulatory compliance, and quality culture built from the development stage enable it to serve as a trusted partner to leading pharmaceutical companies worldwide.In this interview, Mr. Girish Chovatia shares key milestones in Ami Lifesciences’ growth journey, its approach to sustainability and innovation, and vision for expanding into new therapeutic areas and technologies to strengthen their global presence.Ami Lifesciences has grown rapidly since it began API operations in 2006. What have been the key strategic decisions or turning points that have fueled this growth?When we started API operations in 2006, we knew we were entering a highly competitive, globalized market. The key turning points in our journey were rooted in making bold but carefully thought-out strategic decisions. The first was building a quality-first culture from day one. We invested early in strong regulatory systems, which allowed us to secure approvals from agencies like FDA, EDQM and, PMDA, opening global markets.Another major factor was our focus on complex chemistry and high-barrier molecules. Instead of competing only in crowded, generic APIs, we decided to differentiate ourselves by developing technically challenging products where our chemistry expertise could shine.We also expanded our global footprint quickly, entering over 60 countries with a diverse product portfolio. Partnerships with leading pharmaceutical companies gave us both credibility and growth momentum. Each milestone—from our first CEP approval to our first FDA clearance—strengthened our foundation.Most importantly, we built a team that believes in long-term value creation, not shortcuts. That culture of quality, innovation, and customer trust continues to fuel our growth.HIGHLIGHTS// Building quality-first culture/focus on complex chemistry/expanding global footprint/belief in long-term value creationWith 80 APIs and a presence in more than 60 countries, how does Ami Lifesciences ensure regulatory compliance and maintain quality standards across such a diverse global footprint?For us, regulatory compliance is not just a requirement—it is the backbone of our credibility. We’ve built a quality culture that starts from the development stage itself. Our dedicated DQA (Development Quality Assurance) and DRA (Development Regulatory Affairs) teams are involved right from early R&D, ensuring that every molecule is designed with regulatory expectations in mind.All our facilities operate under stringent cGMP (current good manufacturing practices) conditions and are routinely audited by leading authorities, including the FDA, EDQM, PMDA, and multiple global partners. We have built robust systems for documentation, training, and monitoring that keep compliance non-negotiable.Equally important is the mindset—we train our teams to think “compliance-first” in every activity, big or small. Whether it’s a lab scientist, a production engineer, or a QA associate, everyone knows that quality and compliance are paramount.This integration of systems, people and, culture ensures that no matter which market we serve—be it the US, Europe, Japan, or emerging economies—our partners receive products of consistently high standards.HIGHLIGHTS// Compliance backbone of credibility/stringent cGMP conditions/‘compliance-first mindset’/consistency in high standardsHow does Ami Lifesciences’ backward integration across key molecules strengthen cost competitiveness and supply chain assurance for its global clients?Backward integration has been a conscious strategy for us. In today’s environment, customers not only seek high-quality APIs but also security of supply and cost competitiveness. By investing in in-house development and manufacture of key intermediates, we reduce dependency on external vendors and volatile supply chains.This gives us multiple advantages. First, it brings down costs and improves pricing stability, making us a more competitive partner globally. Second, it gives us greater control over timelines—something our clients value tremendously, especially in regulated markets. And third, it ensures resilience; even during global disruptions. We can assure our partners of uninterrupted supply.In a market where reliability is as critical as cost, our backward integration strategy has become a cornerstone of trust and long-term partnerships.HIGHLIGHTS// Backward integration strategy/focus on in-house development/lower costs/control over timelines global footprint/resilience during disruptionsHow is Ami Lifesciences leveraging R&D capabilities and custom synthesis to drive innovation in various therapeutic areas? Our R&D strength has always been at the core of our differentiation. We have over 150 scientists dedicated to developing APIs across complex therapeutic areas such as cardiovascular, anti-diabetic, and central nervous system (CNS) disorders.What sets us apart is our ability to go beyond standard generics. We focus on process innovation—green chemistry, enzymatic applications, and continuous improvement—to make synthesis routes not only cost-effective but also environmentally responsible.Custom synthesis is another pillar. Many of our global partners approach us for tailor-made solutions—whether it’s a new intermediate, a complex chiral molecule, or a high-barrier API. Our flexible R&D infrastructure allows us to design and scale processes efficiently, from grams in the lab to multi-ton manufacturing.By marrying strong chemistry capabilities with customer collaboration, we’ve positioned ourselves as more than a manufacturer—we’re an innovation partner contributing to faster, safer, and more affordable therapies worldwide.HIGHLIGHTS// Strong R&D capabilities/complex therapeutic expertise/green chemistry/custom synthesis solutions/innovation partner for safer therapiesWhat are the next big milestones Ami Lifesciences is targeting in terms of product development and global expansion?Looking ahead, we see the future of Ami Lifesciences in both depth and diversification. On the product side, we are expanding into next-generation therapeutics—with focus areas including oncology APIs, ADC payloads and linkers, short peptides, and select biotechnology platforms. These are high-value, high-science areas where our chemistry expertise and process innovation can create significant impact.We are also investing in platform technologies that can be applied across multiple therapeutic areas, giving us a strategic edge in next-gen molecules.From a global perspective, our milestones include broadening our presence in regulated markets like the US, Europe, and Japan, while simultaneously strengthening our reach in fast-growing markets across Asia, LATAM, and Africa.Our guiding principle is to stay ahead of the curve—building a portfolio and capabilities that align with where global healthcare is heading, not just where it is today.HIGHLIGHTS// Expanding to new-gen therapeutics/investing in platform technologies/broadening presence in regulated markets/staying ahead of the curveCould you elaborate on Ami Lifesciences’ ESG initiatives and how they are integrated into your manufacturing and business strategy?Sustainability is no longer optional—it’s integral to how we do business. At Ami, we’ve made ESG a central pillar of our growth strategy.On the environmental front, we are pioneers in integrating green chemistry and enzymatic applications into our processes. By leveraging biocatalysis, we reduce reliance on harsh chemicals, improve atom economy, and minimize energy usage. Our plants are designed for solvent recovery, water recycling, and energy efficiency, with strong commitments to waste reduction and zero liquid discharge.Socially, we invest heavily in our people and communities. From training and development to ensuring a safe workplace, we believe our people are our greatest asset. Beyond our facilities, we engage in education, healthcare, and environmental initiatives that uplift surrounding communities.On governance, we run with transparency, accountability, and ethics at the forefront. Our systems ensure compliance not just with laws but with global best practices in corporate responsibility.This holistic ESG framework ensures that as we grow, we do so responsibly create value for customers, employees, communities, and the environment alike.HIGHLIGHTS// ESG central to growth strategy/energy and resource efficiency/waste reduction and zero liquid discharge/holistic responsible growthHow does Ami Lifesciences’ manufacturing infrastructure enhance scalability and quality for its clients?Our manufacturing infrastructure is built for both flexibility and scale. Our Karakhadi facility (in Gujarat) is approved by leading agencies such as FDA, EDQM, ANVISA (Brazilian Health Regulatory Agency), NMPA (National Medical Products Administration of China) and KMFDS (Korean Ministry of Food and Drug Safety).Our products are filed in many other regulatory agencies like PMDA, NMPA, Therapeutic Goods Administration and Health Canada; giving our partners complete confidence in compliance and quality.The facility has multi-purpose production blocks, allowing us to handle diverse chemistries and scale projects seamlessly—from grams in the lab to multi-ton commercial quantities. This scalability is a key advantage for customers looking for a partner that can support them across the product lifecycle.We further strengthen supply reliability through backward integration of intermediates, which secures both cost efficiency and supply assurance.What makes us unique is the way we integrate quality and sustainability into manufacturing. By embedding quality from the development stage and incorporating green chemistry and enzymatic processes, we ensure that our output is not only reliable and compliant but also environmentally responsible.This combination of regulatory strength, scalability, and sustainable practices makes Ami a trusted long-term partner for leading pharma companies worldwide.HIGHLIGHTS// Flexible, scalable manufacturing infrastructure/facility approved by leading regulators/multi-purpose production blocks/quality, sustainability integrated into manufacturing 

    Impressions: 3026

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    https://www.pharmacompass.com/speak-pharma/we-are-building-capabilities-to-stay-ahead-of-the-curve-and-align-with-future-needs-of-global-healthcare

    PharmaCompass
    13 Oct 2025
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    VLOG #PharmaReel

    [Sponsored by another company]

    ReelPharmaPartner in End-to-End API ManufacturingPartner in End-to-End API Manufacturing

    Partner in End-to-End API Manufacturing
    Partner in End-to-End API Manufacturing

    reelPartner in End-to-End API Manufacturing

    This PharmaReel showcases Coral Drugs, a global partner in end-to-end API manufacturing with more than 27 years of expertise. Supported by vertically integrated cGMP and ISO-compliant facilities, the company is backed by USFDA and EMA certifications, patents, and advanced micronization capabilities.

    Impressions: 2549

    read-more

    DATA COMPILATION #PharmaFlow

    [Sponsored by another company]
    CDMO Activity Tracker: Veranova, ChemExpress invest in ADC facilities; Cohance to set up oligonucleotide facility in India

    CDMO Activity Tracker: Veranova, ChemExpress invest in ADC facilities; Cohance to set up oligonucleotide facility in India

    The contract development and manufacturing organization (CDMO) sector has emerged as a key partner in new drug development. This was evident from the strategic investments, partnerships, and expansions witnessed in the third quarter (Q3) of 2025. Several CDMOs, such as Cohance Lifesciences, Fermion Oy, Axplora, AGC Pharma Chemicals invested in new projects. Others, including Veranova, Aenova, and Biosynth, expanded capacities, while Ofichem strengthened its footprint with the acquisition of Avivia BV. CDMOs like Fareva, Evonik, and Samsung Biologics forged strategic partnerships for growth. During Q3, the sector continued to adopt artificial intelligence (AI). This prompted the US Food and Drug Administration (FDA) to issue guidance that recognizes the increasing use of AI and data analytics in drug development.  View CDMO Activity Tracker for Q3 2025 (Free Excel Available) Cohance, Veranova invest in bioconjugation suites in US; ChemExpress inks ADC deal Earlier this year, Indian drugmaker Suven Pharmaceuticals Limited merged with  leading CDMO Cohance Lifesciences Limited. The merged entity — Cohance Lifesciences — has invested US$ 10 million in a current Good Manufacturing Practice (cGMP) bioconjugation suite at its subsidiary NJ Bio in Princeton, New Jersey.  NJ Bio is executing a major program for an existing innovator client with multiple antibody-drug conjugate (ADC) candidates. Cohance also announced an INR 230 million (approximately US$ 2.58 million) investment in a cGMP oligonucleotide facility at its Hyderabad (India) site. Veranova’s Devens (Massachusetts) site successfully passed a routine FDA cGMP surveillance inspection with a “No Action Indicated” (NAI) classification. Earlier, the company had initiated a US$ 50 million investment to expand its ADC and bioconjugate capabilities at its Devens site. This includes a 9,000-square-foot facility expansion with a new process development lab, two additional cGMP suites, and state-of-the-art bioconjugation development and manufacturing capabilities. These initiatives strengthen the site’s highly potent API (HPAPI) and ADC development and manufacturing capabilities. Biosynth has expanded its Berlin facility with a new GMP bioconjugation suite. The expansion supports the company’s manufacturing capabilities in conjugate vaccines, conjugate drugs, activated polyethylene glycol (PEGs), and polymer-based drug delivery excipients. ChemExpress, Mabwell Bioscience, and Insilico Medicine have entered into a strategic partnership to jointly develop a large ADC compound library and advance next-generation ADC candidates. The collaboration combines Mabwell’s antibody and ADC technology, Insilico’s AI-powered drug design platform, and ChemExpress’s expertise in linker-payload chemistry. Together, they aim to build a complete, AI-driven ADC development model that accelerates discovery, optimization, and commercialization. This partnership is expected to enhance R&D efficiency and deliver safer, more effective cancer treatments.  View CDMO Activity Tracker for Q3 2025 (Free Excel Available) Fermion, Axplora, Aenova increase API manufacturing capacities; ICE Pharma expands India facility Finnish CDMO Fermion Oy has launched a renovation project at its Hanko (Finland) production site to modernize its API manufacturing capabilities. This expansion is part of Fermion's broader strategy to increase production, enhance flexibility in the manufacturing of both existing and future pharmaceutical products, and enable potential contract manufacturing opportunities. German CDMO Axplora has announced a €6.5 million (approximately US$ 7.5 million) investment to expand its API manufacturing capacity at its Vizag site in India. This expansion aims to strengthen both production capabilities and supply chain resilience. India-based Aarti Pharmalabs has inaugurated the first phase of its greenfield manufacturing facility in Gujarat (India). This expansion aims to bolster Aarti's CDMO and contract manufacturing organization (CMO) services, targeting a revenue goal of INR 10 billion (approximately US$ 112 million). Snapdragon Chemistry, which was acquired by Cambrex in 2023, has expanded its Massachusetts facility to better support peptide drug development and manufacturing. With this upgrade, the company can now handle peptide projects from early development through full-scale manufacturing. Italy-headquartered ICE Pharma has expanded its Raichem facility in India. The new facility will enhance the production of ursodeoxycholic acid (UDCA), an API it derives from chicken bile. This expansion increases the site’s raw UDCA output by 120 metric tons annually. Spain-headquartered AGC Pharma Chemicals inaugurated a new advanced manufacturing plant in Barcelona, with an investment of €110 million (approximately US$ 128.3 million). The plant spans 7,500 square meters and integrates cutting-edge technologies to support the entire drug development lifecycle — from R&D to commercial manufacturing. This represents a 30 percent increase in the company’s production capacity and introduces a segment dedicated to HPAPIs. Germany-headquartered Aenova has launched a new hot melt extrusion platform at its Regensburg (Germany) site. This new equipment enables the production of advanced drug formulations, while handling all testing and quality checks in-house. The move strengthens Aenova’s capabilities in developing and manufacturing complex medications. US-based Cytovance Biologics has introduced in-house formulation development services, enhancing its role as a comprehensive partner for biologic drug developers. These services utilize quality-by-design principles to ensure speed, safety, and precision in current and future client programs.  View CDMO Activity Tracker for Q3 2025 (Free Excel Available)  Ofichem acquires Avivia BV; Evonik, Samsung Biologics form strategic collaborations Europe-based CDMO Ofichem Group announced the acquisition of Avivia BV, a formulation development company in the Netherlands. This acquisition is part of Ofichem’s strategy to become a fully integrated provider of development solutions across both drug substance and drug product, with a focus on complex formulations. Ofichem has also acquired Meribel Pharma Solutions’ site in Uppsala (Sweden) to strengthen its support for biotech innovators and expand its presence in the Nordic region.  Simtra BioPharma Solutions has acquired a 65-acre property near its Bloomington, Indiana (US) facility, adding over 300,000 square feet of potential expansion space. With this site, Simtra now has the flexibility to rapidly expand in the US. German specialty chemicals company Evonik is partnering with German biotech Ethris to develop and commercialize a next-generation lipid nanoparticle (LNP) platform for delivering nucleic acid therapies. Evonik will assist in formulation using Ethris’ SNaP LNP technology. The LNP market alone is projected to grow to US$2.3 billion by 2032. Luxembourg-headquartered Fareva has partnered with Zhaoke Ophthalmology to expand its footprint in China’s pharma market. Zhaoke will act as Fareva’s go-to partner for customers seeking pharmaceutical manufacturing in China. Samsung Biologics has signed a 1.8 trillion won (US$ 1.3 billion) manufacturing agreement with an undisclosed US-based drugmaker. And UK-based eXmoor Pharma has partnered with Anthony Nolan to provide end-to-end services for cell therapy developers.  View CDMO Activity Tracker for Q3 2025 (Free Excel Available)  Our view The global CDMO market, valued at around US$ 255 billion in 2025, is projected to grow to over US$ 465 billion by 2032. Significantly, about 60 percent of new drug approvals in the US and over 65 percent in Europe now involve CDMO support. The developments outlined above underscore the increasing role CDMOs are playing today in bringing about growth and innovation in the pharmaceutical industry.  
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    Impressions: 271

    https://www.pharmacompass.com/radio-compass-blog/cdmo-activity-tracker-veranova-chemexpress-invest-in-adc-facilities-cohance-to-set-up-oligonucleotide-facility-in-india

    #PharmaFlow by PHARMACOMPASS
    16 Oct 2025
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    NEWS #PharmaBuzz

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    Sun Pharma Faces Limited Earnings Impact From Us Tariffs
    Sun Pharma Faces Limited Earnings Impact From Us Tariffs

    28 Sep 2025

    // ECONOMICTIMES

    https://economictimes.indiatimes.com/industry/healthcare/biotech/pharmaceuticals/us-tariffs-only-sun-pharma-exposed-to-some-headline-risk-but-with-limited-earnings-impact/articleshow/124191956.cms

    ECONOMICTIMES
    28 Sep 2025
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    Glenmark, Granules, Zydus Recall Products For Manufacturing Issue
    Glenmark, Granules, Zydus Recall Products For Manufacturing Issue

    28 Sep 2025

    // ECONOMICTIMES

    https://economictimes.indiatimes.com/industry/healthcare/biotech/pharmaceuticals/glenmark-granules-zydus-recall-products-in-us-over-manufacturing-issues-usfda/articleshow/124191236.cms

    ECONOMICTIMES
    28 Sep 2025
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    Enforcement Report - Week of September 24, 2025
    Enforcement Report - Week of September 24, 2025

    24 Sep 2025

    // FDA

    https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-september-24-2025-3088.pdf

    FDA
    24 Sep 2025
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    Adaptability Key For Success In Uncertain Times: Sun Pharma
    Adaptability Key For Success In Uncertain Times: Sun Pharma

    18 Sep 2025

    // ECONOMICTIMES

    https://economictimes.indiatimes.com/industry/healthcare/biotech/pharmaceuticals/adaptability-key-for-success-in-uncertain-times-sun-pharmas-dilip-shanghvi/articleshow/123974059.cms

    ECONOMICTIMES
    18 Sep 2025
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    FDA Finds Sun Pharma's Halol Plant Non-Compliant with Rules
    FDA Finds Sun Pharma's Halol Plant Non-Compliant with Rules

    09 Sep 2025

    // REUTERS

    https://www.reuters.com/business/healthcare-pharmaceuticals/us-fda-deems-sun-pharmas-halol-plant-not-compliant-with-its-manufacturing-rules-2025-09-09/

    REUTERS
    09 Sep 2025
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    Enforcement Report - Week of August 13, 2025
    Enforcement Report - Week of August 13, 2025

    13 Aug 2025

    // FDA

    https://www.pharmacompass.com/pdf/news/enforcement-report-week-of-august-13-2025-91528.pdf

    FDA
    13 Aug 2025
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    ALL APIs

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

    01

    Tramadol Hydrochloride

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

    OTS 2025
    Not Confirmed
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    Tramadol Hydrochloride

    India

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

    arrow
    OTS 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 : 16002

    Submission : 2002-06-06

    Status : Active

    Type : II

     CEP/COS arrow-down
    ✖

    Certificate Number : R1-CEP 2016-003 - Rev 00

    Issue Date : 2022-04-25

    Type : Chemical

    Substance Number : 1681

    Status : Valid

     JDMF arrow-down
    ✖

    Registration Number : 226MF10018

    Registrant's Address : SUN HOUSE, Plot No. 201 B/1, Western Express Highway, Goregaon (E), Mumbai 400063, Maharashtra, India

    Initial Date of Registration : 2014-01-21

    Latest Date of Registration :

    EU-WCarrow-down
    ✖

    Date of Issue : 2025-08-05

    Valid Till : 2028-06-02

    Written Confirmation Number : WC-0011

    Address of the Firm :

    NDC KDMF arrow-down
    ✖

    Registrant Name : Humedics Co., Ltd.

    Registration Date : 2018-01-22

    Registration Number : 20120608-161-I-50-01(7)

    Manufacturer Name : Sun Pharmaceutical Industries Ltd.

    Manufacturer Address : A-7/A-8 MIDC Industrial Area, Ahmednagar, Maharashtra 414111

     VMF Others AUDIT
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    #PipelineProspector

    Market
    Place

    02

    Clarithromycin

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

    OTS 2025
    Not Confirmed
    arrow

    Clarithromycin

    India

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

    arrow
    OTS 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 : 16563

    Submission : 2003-05-02

    Status : Inactive

    Type : II

     CEP/COS arrow-down
    ✖

    Certificate Number : CEP 2006-246 - Rev 05

    Issue Date : 2024-02-15

    Type : Chemical

    Substance Number : 1651

    Status : Valid

     JDMF arrow-down
    ✖

    Registration Number : 220MF10255

    Registrant's Address : Plot No. 90, Sector 32, Gurgaon, Haryana 122 001, India　

    Initial Date of Registration : 2008-12-12

    Latest Date of Registration :

    EU-WCarrow-down
    ✖

    Date of Issue : 2025-07-10

    Valid Till : 2028-07-04

    Written Confirmation Number : WC-0216

    Address of the Firm :

    NDC KDMF VMF Others AUDIT
    blank

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    #PipelineProspector

    Market
    Place

    03

    Gemcitabine

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

    OTS 2025
    Not Confirmed
    arrow

    Gemcitabine

    India

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

    arrow
    OTS 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 : 19427

    Submission : 2006-05-16

    Status : Active

    Type : II

     CEP/COS arrow-down
    ✖

    Certificate Number : CEP 2007-021 - Rev 02

    Issue Date : 2024-06-12

    Type : Chemical

    Substance Number : 2306

    Status : Valid

     JDMF arrow-down
    ✖

    Registration Number : 221MF10018

    Registrant's Address : SUN HOUSE, Plot No. 201 B/1, Western Express Highway, Goregaon (E), Mumbai 400063, Maharashtra, India

    Initial Date of Registration : 2009-01-28

    Latest Date of Registration :

    EU-WCInactive-api
    ✖

    Date of Issue : 2022-06-08

    Valid Till : 2025-07-25

    Written Confirmation Number : WC-0159nA2

    Address of the Firm :

    NDC arrow-down
    ✖

    NDC Package Code : 62756-807

    Start Marketing Date : 2025-03-31

    End Marketing Date : 2026-12-31

    Dosage Form (Strength) : POWDER (25kg/25kg)

    Marketing Category : BULK INGREDIENT

    KDMF arrow-down
    ✖

    Registrant Name : Repure Healthcare Co., Ltd.

    Registration Date : 2021-07-11

    Registration Number : 20210711-86-D-159-24

    Manufacturer Name : Sun Pharmaceutical Industries Ltd.

    Manufacturer Address : A-7/A-8, MIDC Industrial Area, Ahmednagar 414111, Maharashtra State, India

     VMF Others AUDIT
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    04

    Meropenem

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

    OTS 2025
    Not Confirmed
    arrow

    Meropenem

    India

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

    arrow
    OTS 2025
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    USDMF Inactive-api
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 21194

    Submission : 2007-12-24

    Status : Inactive

    Type : II

     CEP/COS arrow-down
    ✖

    Certificate Number : R0-CEP 2018-268 - Rev 01

    Issue Date : 2022-12-19

    Type : Chemical

    Substance Number : 2234

    Status : Valid

     JDMF arrow-down
    ✖

    Registration Number : 220MF10004

    Registrant's Address : SUN HOUSE, Plot No. 201 B/1, Western Express Highway, Goregaon (E), Mumbai 400063, Maharashtra, India

    Initial Date of Registration : 2008-01-09

    Latest Date of Registration :

    EU-WCarrow-down
    ✖

    Date of Issue : 2025-07-10

    Valid Till : 2028-07-04

    Written Confirmation Number : WC-0216

    Address of the Firm :

    NDC KDMF VMF Others AUDIT
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    05

    Midazolam

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

    OTS 2025
    Not Confirmed
    arrow

    Midazolam

    India

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

    arrow
    OTS 2025
    Not Confirmed
    • fda
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    USDMF Inactive-api
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 15170

    Submission : 2000-11-29

    Status : Inactive

    Type : II

     CEP/COS arrow-down
    ✖

    Certificate Number : R1-CEP 2002-059 - Rev 05

    Issue Date : 2021-09-14

    Type : Chemical

    Substance Number : 936

    Status : Valid

     JDMF arrow-down
    ✖

    Registration Number : 219MF10137

    Registrant's Address : SUN HOUSE, Plot No. 201 B/1, Western Express Highway, Goregaon (E), Mumbai 400063, Maharashtra, India

    Initial Date of Registration : 2007-04-18

    Latest Date of Registration :

    EU-WCarrow-down
    ✖

    Date of Issue : 2025-08-05

    Valid Till : 2028-06-02

    Written Confirmation Number : WC-0011

    Address of the Firm :

    NDC KDMF VMF Others AUDIT
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    Place

    06

    Ofloxacin

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

    OTS 2025
    Not Confirmed
    arrow

    Ofloxacin

    India

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

    arrow
    OTS 2025
    Not Confirmed
    • fda
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    USDMF Inactive-api
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 14240

    Submission : 1999-06-25

    Status : Inactive

    Type : II

     CEP/COS arrow-down
    ✖

    Certificate Number : CEP 2000-106 - Rev 10

    Issue Date : 2025-02-17

    Type : Chemical

    Substance Number : 1455

    Status : Valid

     JDMF arrow-down
    ✖

    Registration Number : 217MF11127

    Registrant's Address : Plot No. 90, Sector 32, Gurgaon, Haryana 122 001, India

    Initial Date of Registration : 2005-12-05

    Latest Date of Registration :

    EU-WCarrow-down
    ✖

    Date of Issue : 2025-08-05

    Valid Till : 2028-06-02

    Written Confirmation Number : WC-0011

    Address of the Firm :

    NDC KDMF VMF Others AUDIT
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    Market
    Place

    07

    Desloratadine

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

    OTS 2025
    Not Confirmed
    arrow

    Desloratadine

    India

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

    arrow
    OTS 2025
    Not Confirmed
    • fda
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    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 19014

    Submission : 2005-12-08

    Status : Active

    Type : II

     CEP/COS arrow-down
    ✖

    Certificate Number : CEP 2013-231 - Rev 02

    Issue Date : 2023-11-20

    Type : Chemical

    Substance Number : 2570

    Status : Valid

     JDMF EU-WCarrow-down
    ✖

    Date of Issue : 2025-08-05

    Valid Till : 2028-06-02

    Written Confirmation Number : WC-0011

    Address of the Firm :

    NDC KDMF VMF Others AUDIT
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    Market
    Place

    08

    Metoprolol Tartrate

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

    OTS 2025
    Not Confirmed
    arrow

    Metoprolol Tartrate

    India

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

    arrow
    OTS 2025
    Not Confirmed
    • fda
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    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 15995

    Submission : 2002-05-18

    Status : Active

    Type : II

     CEP/COS arrow-down
    ✖

    Certificate Number : CEP 2000-056 - Rev 07

    Issue Date : 2024-06-26

    Type : Chemical

    Substance Number : 1028

    Status : Valid

     JDMF EU-WCarrow-down
    ✖

    Date of Issue : 2025-08-05

    Valid Till : 2028-06-02

    Written Confirmation Number : WC-0011

    Address of the Firm :

    NDC KDMF VMF Others AUDIT
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    Market
    Place

    09

    Pantoprazole Sodium

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

    OTS 2025
    Not Confirmed
    arrow

    Pantoprazole Sodium

    India

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

    arrow
    OTS 2025
    Not Confirmed
    • fda
    • EDQM
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    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : Reviewed

    Rev. Date : 2019-06-20

    Pay. Date : 2019-06-17

    DMF Number : 17090

    Submission : 2004-01-08

    Status : Active

    Type : II

     CEP/COS arrow-down
    ✖

    Certificate Number : CEP 2008-323 - Rev 05

    Issue Date : 2025-05-28

    Type : Chemical

    Substance Number : 2296

    Status : Valid

     JDMF EU-WCarrow-down
    ✖

    Date of Issue : 2025-08-05

    Valid Till : 2028-06-02

    Written Confirmation Number : WC-0011

    Address of the Firm :

    NDC KDMF VMF Others AUDIT
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    Market
    Place

    10

    Repaglinide

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

    OTS 2025
    Not Confirmed
    arrow

    Repaglinide

    India

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

    arrow
    OTS 2025
    Not Confirmed
    • fda
    • EDQM
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    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 17825

    Submission : 2004-11-10

    Status : Active

    Type : II

     CEP/COS arrow-down
    ✖

    Certificate Number : R1-CEP 2006-069 - Rev 02

    Issue Date : 2015-05-26

    Type : Chemical

    Substance Number : 2135

    Status : Valid

     JDMF EU-WCarrow-down
    ✖

    Date of Issue : 2025-08-05

    Valid Till : 2028-06-02

    Written Confirmation Number : WC-0011

    Address of the Firm :

    NDC KDMF VMF Others AUDIT
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    Market
    Place

    Only 10 entries up to this point, click to access all click full view read-more
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    FDA Orange Book

    read-more
    read-more

    01

    Brand Name : YONSA

    India
    Aus. Peptide Conference
    Not Confirmed
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    Brand Name : YONSA

    India
    Aus. Peptide Conference
    Not Confirmed
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    • fda
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    RLD : Yes

    TE Code :

    ABIRATERONE ACETATE

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET; ORAL

    Proprietary Name : YONSA

    Dosage Strength : 125MG

    Approval Date : 2018-05-22

    Application Number : 210308

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    Market
    Place

    02

    Brand Name : ACETAMINOPHEN

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow

    Brand Name : ACETAMINOPHEN

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow
    • fda
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    RLD : No

    TE Code :

    ACETAMINOPHEN

    Sun Pharmaceutical Industries Limited

    Dosage Form : SUPPOSITORY; RECTAL

    Proprietary Name : ACETAMINOPHEN

    Dosage Strength : 120MG

    Approval Date : 1995-02-27

    Application Number : 73106

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    Market
    Place

    03

    Brand Name : ACETAMINOPHEN

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow

    Brand Name : ACETAMINOPHEN

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow
    • fda
    • EDQM
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    RLD : No

    TE Code :

    ACETAMINOPHEN

    Sun Pharmaceutical Industries Limited

    Dosage Form : SUPPOSITORY; RECTAL

    Proprietary Name : ACETAMINOPHEN

    Dosage Strength : 325MG

    Approval Date : 1995-02-27

    Application Number : 73107

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    Market
    Place

    04

    Brand Name : ACETAMINOPHEN

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow

    Brand Name : ACETAMINOPHEN

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    ACETAMINOPHEN

    Sun Pharmaceutical Industries Limited

    Dosage Form : SUPPOSITORY; RECTAL

    Proprietary Name : ACETAMINOPHEN

    Dosage Strength : 650MG

    Approval Date : 1995-02-27

    Application Number : 73108

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    Market
    Place

    05

    Brand Name : ACETAMINOPHEN

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow

    Brand Name : ACETAMINOPHEN

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    ACETAMINOPHEN

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : ACETAMINOPHEN

    Dosage Strength : 650MG

    Approval Date : 2002-03-19

    Application Number : 76200

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

    blank

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    Market
    Place

    06

    Brand Name : ACETAMINOPHEN

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow

    Brand Name : ACETAMINOPHEN

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow
    • fda
    • EDQM
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    RLD : No

    TE Code :

    ACETAMINOPHEN

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : ACETAMINOPHEN

    Dosage Strength : 650MG

    Approval Date : 2011-12-14

    Application Number : 78569

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    Market
    Place

    07

    Brand Name : ACETAMINOPHEN

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow

    Brand Name : ACETAMINOPHEN

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    ACETAMINOPHEN

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : ACETAMINOPHEN

    Dosage Strength : 650MG

    Approval Date : 2009-11-18

    Application Number : 90205

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    Market
    Place

    08

    Brand Name : BUTALBITAL, ACETAMIN...

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow

    Brand Name : BUTALBITAL, ACETAMIN...

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow
    • fda
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    RLD : No

    TE Code :

    ACETAMINOPHEN; BUTALBITAL; CAFFEINE

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET; ORAL

    Proprietary Name : BUTALBITAL, ACETAMINOPHE...

    Dosage Strength : 325MG;50MG;40MG

    Approval Date : 2001-07-23

    Application Number : 40390

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    Market
    Place

    09

    Brand Name : BUTALBITAL, ACETAMIN...

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow

    Brand Name : BUTALBITAL, ACETAMIN...

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow
    • fda
    • EDQM
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    RLD : No

    TE Code :

    ACETAMINOPHEN; BUTALBITAL; CAFFEINE

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET; ORAL

    Proprietary Name : BUTALBITAL, ACETAMINOPHE...

    Dosage Strength : 500MG;50MG;40MG

    Approval Date : 2001-07-23

    Application Number : 40394

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    Market
    Place

    10

    Brand Name : BUTALBITAL, ACETAMIN...

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow

    Brand Name : BUTALBITAL, ACETAMIN...

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    ACETAMINOPHEN; BUTALBITAL; CAFFEINE

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET; ORAL

    Proprietary Name : BUTALBITAL, ACETAMINOPHE...

    Dosage Strength : 325MG;50MG;40MG

    Approval Date : 2005-07-29

    Application Number : 40601

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    Market
    Place

    Only 10 entries up to this point, click to access all click full view read-more
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    Europe

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    01

    Brand Name : Sertraline Sun

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow

    Brand Name : Sertraline Sun

    India
    arrow
    Aus. Peptide Conference
    Not Confirmed
    • fda
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    Regulatory Info : Approved

    Registration Country : Sweden

    Sertraline Hydrochloride

    Sun Pharmaceutical Industries Limited

    Dosage Form : Film Coated Tablet

    Dosage Strength : 100mg

    Packaging :

    Brand Name : Sertraline Sun

    Approval Date : 05/11/2004

    Application Number : 20040607005620

    Regulatory Info : Approved

    Registration Country : Sweden

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    Market
    Place

    02

    Brand Name : Sertraline Sun

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow

    Brand Name : Sertraline Sun

    India
    arrow
    Aus. Peptide Conference
    Not Confirmed
    • fda
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    Regulatory Info : Approved

    Registration Country : Sweden

    Sertraline Hydrochloride

    Sun Pharmaceutical Industries Limited

    Dosage Form : Film Coated Tablet

    Dosage Strength : 50mg

    Packaging :

    Brand Name : Sertraline Sun

    Approval Date : 05/11/2004

    Application Number : 20040607005613

    Regulatory Info : Approved

    Registration Country : Sweden

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    Market
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    03

    Brand Name : Abacavir/Lamivudina ...

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow

    Brand Name : Abacavir/Lamivudina ...

    India
    arrow
    Aus. Peptide Conference
    Not Confirmed
    • fda
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    Regulatory Info : Cancelled

    Registration Country : Spain

    Abacavir Sulfate; Lamivudine

    Sun Pharmaceutical Industries Limited

    Dosage Form : Film Coated Tablet

    Dosage Strength : 600MG; 300 MG

    Packaging :

    Brand Name : Abacavir/Lamivudina Sun

    Approval Date : 2019-07-16

    Application Number : 84367

    Regulatory Info : Cancelled

    Registration Country : Spain

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    Market
    Place

    04

    Brand Name : Abiraterona Sun

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow

    Brand Name : Abiraterona Sun

    India
    arrow
    Aus. Peptide Conference
    Not Confirmed
    • fda
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    • WHO-GMP
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    Regulatory Info : Authorized

    Registration Country : Spain

    Abiraterone Acetate

    Sun Pharmaceutical Industries Limited

    Dosage Form : Film Coated Tablet

    Dosage Strength : 500MG

    Packaging :

    Brand Name : Abiraterona Sun

    Approval Date : 2022-09-09

    Application Number : 88075

    Regulatory Info : Authorized

    Registration Country : Spain

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    Market
    Place

    05

    Brand Name : Acyclovir Sun

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow

    Brand Name : Acyclovir Sun

    India
    arrow
    Aus. Peptide Conference
    Not Confirmed
    • fda
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    Regulatory Info : Approved

    Registration Country : Sweden

    Acyclovir

    Sun Pharmaceutical Industries Limited

    Dosage Form : Tablet

    Dosage Strength : 200mg

    Packaging :

    Brand Name : Acyclovir Sun

    Approval Date : 1999-09-24

    Application Number : 19990924000218

    Regulatory Info : Approved

    Registration Country : Sweden

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    Market
    Place

    06

    Brand Name : Acyclovir Sun

    India
    Aus. Peptide Conference
    Not Confirmed
    arrow

    Brand Name : Acyclovir Sun

    India
    arrow
    Aus. Peptide Conference
    Not Confirmed
    • fda
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    Regulatory Info : Approved

    Registration Country : Sweden

    Acyclovir

    Sun Pharmaceutical Industries Limited

    Dosage Form : Tablet

    Dosage Strength : 400mg

    Packaging :

    Brand Name : Acyclovir Sun

    Approval Date : 1999-09-24

    Application Number : 19990924000225

    Regulatory Info : Approved

    Registration Country : Sweden

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    Regulatory Info : Approved

    Registration Country : Sweden

    Acyclovir

    Sun Pharmaceutical Industries Limited

    Dosage Form : Tablet

    Dosage Strength : 800mg

    Packaging :

    Brand Name : Acyclovir Sun

    Approval Date : 1999-09-24

    Application Number : 19990924000232

    Regulatory Info : Approved

    Registration Country : Sweden

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    Brand Name : Acyclovir

    India
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    Regulatory Info :

    Registration Country : Italy

    Acyclovir Sodium

    Sun Pharmaceutical Industries Limited

    Dosage Form : Aciclovir 8% 100Ml Oral Use

    Dosage Strength : os suspe 100 ml 8%

    Packaging :

    Brand Name : Acyclovir

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Italy

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    Regulatory Info :

    Registration Country : Italy

    Acyclovir Sodium

    Sun Pharmaceutical Industries Limited

    Dosage Form : Acyclovir 400Mg 25 Units' Oral...

    Dosage Strength : 25 CPR 400 mg

    Packaging :

    Brand Name : Acyclovir

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Italy

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    Regulatory Info :

    Registration Country : Italy

    Acyclovir Sodium

    Sun Pharmaceutical Industries Limited

    Dosage Form : Acyclovir 800Mg 35 Joined' Ora...

    Dosage Strength : 35 CPR 800 mg

    Packaging :

    Brand Name : Acyclovir

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Italy

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    01

    POLY (LACTIC-CO-GLYCOLIC ACID) (PLG...

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

    Aus. Peptide Conference
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    POLY (LACTIC-CO-GLYCOLIC ACID) (PLG...

    India

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

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    USDMF arrow-down Click Us! arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 39685

    Submission : 2024-03-29

    Status : Active

    Type : IV

     CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
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    [DL]-POLYLACTIC ACID OR [DL]-PLA-2

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

    Aus. Peptide Conference
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    [DL]-POLYLACTIC ACID OR [DL]-PLA-2

    India

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

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    USDMF arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 40876

    Submission : 2025-03-26

    Status : Active

    Type : IV

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

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

    Aus. Peptide Conference
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    Hypromellose Phthalate

    India

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

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    USDMF Inactive-api
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 17589

    Submission : 2004-08-06

    Status : Inactive

    Type : IV

     CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
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    Contact Sun Pharmaceutical Industries Limited and get a quotation

    Sun Pharmaceutical Industries Limited is a supplier offers 396 products (APIs, Excipients or Intermediates).

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