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01 1M/sIPCA Laboratories Limited
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01 1Estradiol Valerate EP/BP/USP
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01 1WC-0402A2
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01 1India
Date of Issue : 2020-09-08
Valid Till : 2023-04-24
Written Confirmation Number : WC-0402A2
Address of the Firm : Plot no. 23-24 GIDC Estate Nandesari-391340 Dist Vadodara Gujarat
42
PharmaCompass offers a list of Estradiol Valerate 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 Estradiol Valerate manufacturer or Estradiol Valerate supplier for your needs.
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PharmaCompass also assists you with knowing the Estradiol Valerate API Price utilized in the formulation of products. Estradiol Valerate API Price is not always fixed or binding as the Estradiol Valerate Price is obtained through a variety of data sources. The Estradiol Valerate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Neofollin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neofollin, including repackagers and relabelers. The FDA regulates Neofollin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neofollin 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 Neofollin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Neofollin supplier is an individual or a company that provides Neofollin active pharmaceutical ingredient (API) or Neofollin finished formulations upon request. The Neofollin suppliers may include Neofollin API manufacturers, exporters, distributors and traders.
click here to find a list of Neofollin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Neofollin written confirmation (Neofollin WC) is an official document issued by a regulatory agency to a Neofollin manufacturer, verifying that the manufacturing facility of a Neofollin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Neofollin APIs or Neofollin finished pharmaceutical products to another nation, regulatory agencies frequently require a Neofollin WC (written confirmation) as part of the regulatory process.
click here to find a list of Neofollin suppliers with Written Confirmation (WC) on PharmaCompass.
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