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 (1)
02 Aarti Drugs (1)
03 Apotex Pharmachem (1)
04 Aurobindo Pharma Limited (1)
05 Aurore Life Sciences (1)
06 Cadila Pharmaceuticals (1)
07 Cambrex Corporation (1)
08 Cipla (2)
09 Erregierre SpA (1)
10 Glochem Industries (1)
11 Hetero Drugs (1)
12 Olon S.p.A (1)
13 Raks Pharma (1)
14 Sichuan Xieli Pharmaceutical (1)
15 Teva API (2)
01 RALOXIFENE HYDROCHLORIDE (7)
02 RALOXIFENE HYDROCHLORIDE BULK DRUG SUBSTANCE (1)
03 RALOXIFENE HYDROCHLORIDE USP (7)
04 RALOXIFENE HYDROCHLORIDE USP (NON-STERILE DRUG SUBSTANCE) (1)
05 RALOXIFENE HYDROCHLORIDE, USP (1)
01 Canada (1)
02 China (1)
03 India (10)
04 Israel (2)
05 Italy (2)
06 U.S.A (1)
01 Active (12)
02 Inactive (5)
01 Complete (10)
02 Blank (7)
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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 DMF (Drug Master File) is a document detailing the whole manufacturing process of Evista active pharmaceutical ingredient (API) in detail. Different forms of Evista DMFs exist exist since differing nations have different regulations, such as Evista USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Evista DMF submitted to regulatory agencies in the US is known as a USDMF. Evista USDMF includes data on Evista's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Evista USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Evista suppliers with USDMF on PharmaCompass.
We have 15 companies offering Evista
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