Market Place
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations. 
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01 DR. REDDY'S LABORATORIES LIMITED Hyderabad IN (1)
02 APITORIA PHARMA PRIVATE LIMITED Hyderabad IN (1)
03 APOTEX PHARMACHEM INDIA PVT. LTD Bangalore IN (1)
04 AURORE LIFE SCIENCES PRIVATE LIMITED Hyderabad IN (1)
05 EXCELLA GMBH Feucht DE (1)
06 Erregierre S.p.A. San Paolo D'Argon IT (1)
07 GLOCHEM INDUSTRIES PRIVATE LIMITED Hyderabad IN (2)
08 HETERO DRUGS LIMITED Hyderabad IN (1)
09 KYONGBO PHARMACEUTICAL CO., LTD. Asan-si KR (1)
10 OLON S.P.A. Rodano IT (1)
01 Raloxifene hydrochloride (10)
02 Raloxifene hydrochloride, LAXAI (1)
01 Canada (1)
02 Germany (1)
03 India (6)
04 Italy (2)
05 South Korea (1)
01 Expired (1)
02 Valid (9)
03 Withdrawn by Holder (1)
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PharmaCompass offers a list of Raloxifene Hydrochloride 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 Raloxifene Hydrochloride manufacturer or Raloxifene Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Raloxifene Hydrochloride manufacturer or Raloxifene Hydrochloride supplier.
PharmaCompass also assists you with knowing the Raloxifene Hydrochloride API Price utilized in the formulation of products. Raloxifene Hydrochloride API Price is not always fixed or binding as the Raloxifene Hydrochloride Price is obtained through a variety of data sources. The Raloxifene Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Evista manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Evista, including repackagers and relabelers. The FDA regulates Evista manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Evista 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 Evista manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Evista supplier is an individual or a company that provides Evista active pharmaceutical ingredient (API) or Evista finished formulations upon request. The Evista suppliers may include Evista API manufacturers, exporters, distributors and traders.
click here to find a list of Evista suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Evista CEP of the European Pharmacopoeia monograph is often referred to as a Evista Certificate of Suitability (COS). The purpose of a Evista CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Evista EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Evista to their clients by showing that a Evista CEP has been issued for it. The manufacturer submits a Evista CEP (COS) as part of the market authorization procedure, and it takes on the role of a Evista CEP holder for the record. Additionally, the data presented in the Evista CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Evista DMF.
A Evista CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Evista 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 Evista suppliers with CEP (COS) on PharmaCompass.
We have 9 companies offering Evista
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