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API SUPPLIERS
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Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
About the Company : Polpharma API, part of a leading Polish pharmaceutical group, has over 70 years of experience in process development and cGMP manufacturing. We offer end-to-end solutions, from API...
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
About the Company : Biophore, founded in 2007, has established itself as a reliable partner in the development and manufacturing of niche and complex pharmaceutical products. With 4 USFDA and EU-appro...
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
About the Company : LGM Pharma is a global leader in sourcing hard-to-find APIs and intermediates for the pharmaceutical and biotech industries. LGM is also a full service CDMO providing formulation, ...
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
About the Company : Established in 2004, Metrochem API is one of the fastest-growing APIs, pellets & intermediates manufacturers. It has 6 dedicated manufacturing facilities for its 3 core product gro...
HRV Pharma - Market Expansion Leader in Pharmaceuticals.
About the Company : HRV Pharma is a leading global manufacturer, seller & exporter of a wide range of APIs, advanced intermediates, pellets, food grade chemicals, food additives & food ingredients. It...
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
About the Company : Founded in 1935, TAPI Technology & API Services has a long-standing tradition of advancing health through innovation and dedication. Today, we proudly build upon this legacy, drivi...
Honour is a leading global CDMO and specialty chemicals manufacturer with seven world-class sites delivering quality-driven solutions.
About the Company : Honour is a leading global CDMO and a trusted manufacturer of specialty chemicals and ingredients. With seven world-class facilities built to meet global safety and quality standar...
Qingmu Pharma: Patients first, FDA/CEP/US-DMF/US-VMF/ASMF APIs for Humans & Vets in 100+ countries.
About the Company : Sichuan Qingmu Pharmaceutical Co., Ltd. is an innovation-driven pharmaceutical company focused on regulated markets. We specialize in the R&D and manufacturing of generic APIs and ...
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DOSAGE - TABLET;ORAL - 0.25MG
USFDA APPLICATION NUMBER - 205422
DOSAGE - TABLET;ORAL - 0.5MG
USFDA APPLICATION NUMBER - 205422
DOSAGE - TABLET;ORAL - 1MG
USFDA APPLICATION NUMBER - 205422
DOSAGE - TABLET;ORAL - 2MG
USFDA APPLICATION NUMBER - 205422
DOSAGE - TABLET;ORAL - 3MG
USFDA APPLICATION NUMBER - 205422
DOSAGE - TABLET;ORAL - 4MG
USFDA APPLICATION NUMBER - 205422
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ABOUT THIS PAGE
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PharmaCompass offers a list of Brexpiprazole API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Brexpiprazole manufacturer or Brexpiprazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Brexpiprazole manufacturer or Brexpiprazole supplier.
PharmaCompass also assists you with knowing the Brexpiprazole API Price utilized in the formulation of products. Brexpiprazole API Price is not always fixed or binding as the Brexpiprazole Price is obtained through a variety of data sources. The Brexpiprazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AKOS025291100 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AKOS025291100, including repackagers and relabelers. The FDA regulates AKOS025291100 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AKOS025291100 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of AKOS025291100 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AKOS025291100 supplier is an individual or a company that provides AKOS025291100 active pharmaceutical ingredient (API) or AKOS025291100 finished formulations upon request. The AKOS025291100 suppliers may include AKOS025291100 API manufacturers, exporters, distributors and traders.
click here to find a list of AKOS025291100 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A AKOS025291100 DMF (Drug Master File) is a document detailing the whole manufacturing process of AKOS025291100 active pharmaceutical ingredient (API) in detail. Different forms of AKOS025291100 DMFs exist exist since differing nations have different regulations, such as AKOS025291100 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A AKOS025291100 DMF submitted to regulatory agencies in the US is known as a USDMF. AKOS025291100 USDMF includes data on AKOS025291100's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The AKOS025291100 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of AKOS025291100 suppliers with USDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a AKOS025291100 Drug Master File in Korea (AKOS025291100 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of AKOS025291100. The MFDS reviews the AKOS025291100 KDMF as part of the drug registration process and uses the information provided in the AKOS025291100 KDMF to evaluate the safety and efficacy of the drug.
After submitting a AKOS025291100 KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their AKOS025291100 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of AKOS025291100 suppliers with KDMF on PharmaCompass.
A AKOS025291100 written confirmation (AKOS025291100 WC) is an official document issued by a regulatory agency to a AKOS025291100 manufacturer, verifying that the manufacturing facility of a AKOS025291100 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting AKOS025291100 APIs or AKOS025291100 finished pharmaceutical products to another nation, regulatory agencies frequently require a AKOS025291100 WC (written confirmation) as part of the regulatory process.
click here to find a list of AKOS025291100 suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing AKOS025291100 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for AKOS025291100 API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture AKOS025291100 as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain AKOS025291100 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a AKOS025291100 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of AKOS025291100 suppliers with NDC on PharmaCompass.
AKOS025291100 Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of AKOS025291100 GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right AKOS025291100 GMP manufacturer or AKOS025291100 GMP API supplier for your needs.
A AKOS025291100 CoA (Certificate of Analysis) is a formal document that attests to AKOS025291100's compliance with AKOS025291100 specifications and serves as a tool for batch-level quality control.
AKOS025291100 CoA mostly includes findings from lab analyses of a specific batch. For each AKOS025291100 CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
AKOS025291100 may be tested according to a variety of international standards, such as European Pharmacopoeia (AKOS025291100 EP), AKOS025291100 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (AKOS025291100 USP).
