DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 2DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
02 2APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
03 2CIPLA LIMITED Mumbai IN
04 2CURIA SPAIN S.A.U. Boecillo ES
05 1HETERO LABS LIMITED Hyderabad IN
06 1Hubei Gedian Humanwell Pharmaceutical Co., Ltd. E-Zhou CN
07 1MSN LABORATORIES PRIVATE LIMITED Rudraram Village IN
08 1STERLING S.p.A. Solomeo Di Corciano IT
01 6Finasteride
02 1Finasteride, BSA Route - I Code
03 1Finasteride, EAA route
04 1Finasteride, Form I
05 1Finasteride, Form III
06 1Finasteride, Form-I
07 1Finasteride, Process A
01 1China
02 8India
03 1Italy
04 2Spain
01 1Expired
02 10Valid
03 1Withdrawn by Holder
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
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
Certificate Number : CEP 2006-254 - Rev 05
Status : Valid
Issue Date : 2023-11-16
Type : Chemical
Substance Number : 1615
Certificate Number : CEP 2016-219 - Rev 02
Status : Valid
Issue Date : 2024-09-26
Type : Chemical
Substance Number : 1615
Certificate Number : R1-CEP 2005-025 - Rev 05
Status : Valid
Issue Date : 2022-04-12
Type : Chemical
Substance Number : 1615
Certificate Number : R1-CEP 2004-255 - Rev 01
Status : Valid
Issue Date : 2021-08-24
Type : Chemical
Substance Number : 1615
Certificate Number : R1-CEP 2011-043 - Rev 01
Status : Valid
Issue Date : 2021-08-25
Type : Chemical
Substance Number : 1615
Certificate Number : CEP 2011-351 - Rev 03
Status : Valid
Issue Date : 2024-11-04
Type : Chemical
Substance Number : 1615
Certificate Number : R1-CEP 2013-238 - Rev 00
Status : Valid
Issue Date : 2020-05-28
Type : Chemical
Substance Number : 1615
Certificate Number : R1-CEP 2008-024 - Rev 04
Status : Valid
Issue Date : 2019-08-06
Type : Chemical
Substance Number : 1615
Certificate Number : R1-CEP 2008-130 - Rev 01
Status : Valid
Issue Date : 2017-12-14
Type : Chemical
Substance Number : 1615
77
PharmaCompass offers a list of Finasteride 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 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.
PharmaCompass also assists you with knowing the Finasteride API Price utilized in the formulation of products. Finasteride API Price is not always fixed or binding as the Finasteride Price is obtained through a variety of data sources. The Finasteride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Finasterida manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Finasterida, including repackagers and relabelers. The FDA regulates Finasterida manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Finasterida 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 Finasterida manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Finasterida supplier is an individual or a company that provides Finasterida active pharmaceutical ingredient (API) or Finasterida finished formulations upon request. The Finasterida suppliers may include Finasterida API manufacturers, exporters, distributors and traders.
click here to find a list of Finasterida suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Finasterida CEP of the European Pharmacopoeia monograph is often referred to as a Finasterida Certificate of Suitability (COS). The purpose of a Finasterida CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Finasterida EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Finasterida to their clients by showing that a Finasterida CEP has been issued for it. The manufacturer submits a Finasterida CEP (COS) as part of the market authorization procedure, and it takes on the role of a Finasterida CEP holder for the record. Additionally, the data presented in the Finasterida CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Finasterida DMF.
A Finasterida CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Finasterida 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 Finasterida suppliers with CEP (COS) on PharmaCompass.
We have 8 companies offering Finasterida
Get in contact with the supplier of your choice:
