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01 1M/s Anthem Biosciences Private Limited
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01 1Zavegepant Hydrochloride IH
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01 1WC-0536
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01 1India
Date of Issue : 2022-09-16
Valid Till : 2025-09-15
Written Confirmation Number : WC-0536
Address of the Firm : #49, F1 & F2, Canara Bank Road, Bommasandra Industrial area, Phase 1, Bommasandr...
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PharmaCompass offers a list of Vazegepant 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 Vazegepant manufacturer or Vazegepant supplier for your needs.
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PharmaCompass also assists you with knowing the Vazegepant API Price utilized in the formulation of products. Vazegepant API Price is not always fixed or binding as the Vazegepant Price is obtained through a variety of data sources. The Vazegepant Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A BHV-3500 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BHV-3500, including repackagers and relabelers. The FDA regulates BHV-3500 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BHV-3500 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 BHV-3500 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A BHV-3500 supplier is an individual or a company that provides BHV-3500 active pharmaceutical ingredient (API) or BHV-3500 finished formulations upon request. The BHV-3500 suppliers may include BHV-3500 API manufacturers, exporters, distributors and traders.
click here to find a list of BHV-3500 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A BHV-3500 written confirmation (BHV-3500 WC) is an official document issued by a regulatory agency to a BHV-3500 manufacturer, verifying that the manufacturing facility of a BHV-3500 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting BHV-3500 APIs or BHV-3500 finished pharmaceutical products to another nation, regulatory agencies frequently require a BHV-3500 WC (written confirmation) as part of the regulatory process.
click here to find a list of BHV-3500 suppliers with Written Confirmation (WC) on PharmaCompass.
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