Market Place
Hubei Gedian Humanwell focuses on R&D, production, & sales of fertility regulation drugs & steroidal APIs. 
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01 Hubei Gedian Humanwell Pharmaceutical Co., Ltd. E-Zhou CN (1)
02 DR. REDDY'S LABORATORIES LIMITED Hyderabad IN (2)
03 APITORIA PHARMA PRIVATE LIMITED Hyderabad IN (2)
04 CIPLA LIMITED Mumbai IN (2)
05 CURIA SPAIN S.A.U. Boecillo ES (2)
06 HETERO LABS LIMITED Hyderabad IN (1)
07 MSN LABORATORIES PRIVATE LIMITED Rudraram Village IN (1)
08 STERLING S.p.A. Solomeo Di Corciano IT (1)
01 Finasteride (7)
02 Finasteride, BSA Route - I Code (1)
03 Finasteride, EAA route (1)
04 Finasteride, Form I (1)
05 Finasteride, Form III (1)
06 Finasteride, Process A (1)
01 China (1)
02 India (8)
03 Italy (1)
04 Spain (2)
01 Expired (1)
02 Valid (10)
03 Withdrawn by Holder (1)
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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, 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 Prestwick3_000717 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prestwick3_000717, including repackagers and relabelers. The FDA regulates Prestwick3_000717 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prestwick3_000717 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 Prestwick3_000717 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Prestwick3_000717 supplier is an individual or a company that provides Prestwick3_000717 active pharmaceutical ingredient (API) or Prestwick3_000717 finished formulations upon request. The Prestwick3_000717 suppliers may include Prestwick3_000717 API manufacturers, exporters, distributors and traders.
click here to find a list of Prestwick3_000717 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Prestwick3_000717 CEP of the European Pharmacopoeia monograph is often referred to as a Prestwick3_000717 Certificate of Suitability (COS). The purpose of a Prestwick3_000717 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Prestwick3_000717 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Prestwick3_000717 to their clients by showing that a Prestwick3_000717 CEP has been issued for it. The manufacturer submits a Prestwick3_000717 CEP (COS) as part of the market authorization procedure, and it takes on the role of a Prestwick3_000717 CEP holder for the record. Additionally, the data presented in the Prestwick3_000717 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Prestwick3_000717 DMF.
A Prestwick3_000717 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Prestwick3_000717 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 Prestwick3_000717 suppliers with CEP (COS) on PharmaCompass.
We have 8 companies offering Prestwick3_000717
Get in contact with the supplier of your choice:
