Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
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01 1M/s. Vamsi Lab Ltd.,
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01 1Fenoterol Hydrobromide EP
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01 1WC-0155
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01 1India
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
Date of Issue : 2022-06-13
Valid Till : 2025-07-02
Written Confirmation Number : WC-0155
Address of the Firm : A-14 & 15, MIDC Area, Chincholi, Solapur – 413 255, Maharashtra, India
97
PharmaCompass offers a list of Fenoterol Hydrobromide 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 Fenoterol Hydrobromide manufacturer or Fenoterol Hydrobromide supplier for your needs.
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PharmaCompass also assists you with knowing the Fenoterol Hydrobromide API Price utilized in the formulation of products. Fenoterol Hydrobromide API Price is not always fixed or binding as the Fenoterol Hydrobromide Price is obtained through a variety of data sources. The Fenoterol Hydrobromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Berotek manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Berotek, including repackagers and relabelers. The FDA regulates Berotek manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Berotek API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Berotek supplier is an individual or a company that provides Berotek active pharmaceutical ingredient (API) or Berotek finished formulations upon request. The Berotek suppliers may include Berotek API manufacturers, exporters, distributors and traders.
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A Berotek written confirmation (Berotek WC) is an official document issued by a regulatory agency to a Berotek manufacturer, verifying that the manufacturing facility of a Berotek active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Berotek APIs or Berotek finished pharmaceutical products to another nation, regulatory agencies frequently require a Berotek WC (written confirmation) as part of the regulatory process.
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