Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
01 1M/s. Vamsi Lab Ltd.,
01 1Fenoterol Hydrobromide EP
01 1WC-0155
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
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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 Partusisten manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Partusisten, including repackagers and relabelers. The FDA regulates Partusisten manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Partusisten 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 Partusisten supplier is an individual or a company that provides Partusisten active pharmaceutical ingredient (API) or Partusisten finished formulations upon request. The Partusisten suppliers may include Partusisten API manufacturers, exporters, distributors and traders.
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A Partusisten written confirmation (Partusisten WC) is an official document issued by a regulatory agency to a Partusisten manufacturer, verifying that the manufacturing facility of a Partusisten active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Partusisten APIs or Partusisten finished pharmaceutical products to another nation, regulatory agencies frequently require a Partusisten WC (written confirmation) as part of the regulatory process.
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