DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
02 2CURIA SPAIN S.A.U. Boecillo ES
03 2APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 2CIPLA LIMITED Mumbai IN
05 1HETERO LABS LIMITED Hyderabad IN
06 1HUBEI GEDIAN HUMANWELL PHARMACEUTICAL CO., LTD. Ezhou City CN
07 1MSN LABORATORIES PRIVATE LIMITED Rudraram Village IN
08 1SHAKTI LIFESCIENCE PRIVATE LIMITED Mumbai IN
09 1STERLING S.p.A. Solomeo Di Corciano IT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Certificate Number : R1-CEP 2009-195 - Rev 03
Status : Valid
Issue Date : 2023-07-12
Type : Chemical
Substance Number : 1615
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
Certificate Number : R1-CEP 2004-255 - Rev 01
Status : Valid
Issue Date : 2021-08-24
Type : Chemical
Substance Number : 1615
Curia - Accelerating therapies from discovery to commercialization with flexible, scalable CDMO solutions.
Certificate Number : R1-CEP 2011-043 - Rev 01
Status : Valid
Issue Date : 2021-08-25
Type : Chemical
Substance Number : 1615
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PharmaCompass offers a list of Finasteride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Finasteride manufacturer or Finasteride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Finasteride manufacturer or Finasteride supplier.
A Propecia manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Propecia, including repackagers and relabelers. The FDA regulates Propecia manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Propecia 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 Propecia manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Propecia supplier is an individual or a company that provides Propecia active pharmaceutical ingredient (API) or Propecia finished formulations upon request. The Propecia suppliers may include Propecia API manufacturers, exporters, distributors and traders.
click here to find a list of Propecia suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Propecia CEP of the European Pharmacopoeia monograph is often referred to as a Propecia Certificate of Suitability (COS). The purpose of a Propecia CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Propecia EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Propecia to their clients by showing that a Propecia CEP has been issued for it. The manufacturer submits a Propecia CEP (COS) as part of the market authorization procedure, and it takes on the role of a Propecia CEP holder for the record. Additionally, the data presented in the Propecia CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Propecia DMF.
A Propecia CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Propecia CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Propecia suppliers with CEP (COS) on PharmaCompass.
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