Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
01 1M/s. Vamsi Lab Ltd.,
02 1M/s Melody Healthcare Pvt Ltd
03 1M/s.Cipla Limited
01 1Tiotropium Bromide Hydrate EP/BP
02 1Tiotropium Bromide Monohydrate BP/EP
03 1Tiotropium Bromide Monohydrate EP
01 1WC-0144nA2
02 1WC-0155
03 1WC-0227n
01 3India
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
Tiotropium Bromide Monohydrate EP
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
Tiotropium Bromide Monohydrate BP/EP
Date of Issue : 2022-06-08
Valid Till : 2025-09-08
Written Confirmation Number : WC-0144nA2
Address of the Firm : D-7, MIDC, Industrial Area, Kurkumbh, Taluka: Daund, District: Pune -Zone4- 413 ...
Tiotropium Bromide Hydrate EP/BP
Date of Issue : 2022-07-28
Valid Till : 2025-07-02
Written Confirmation Number : WC-0227n
Address of the Firm : Plot No. J-73, MIDC, Tarapur, Boisar, Dist- Palghar 401506, Maharashtra, India
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A Respimat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Respimat, including repackagers and relabelers. The FDA regulates Respimat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Respimat 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 Respimat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Respimat supplier is an individual or a company that provides Respimat active pharmaceutical ingredient (API) or Respimat finished formulations upon request. The Respimat suppliers may include Respimat API manufacturers, exporters, distributors and traders.
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A Respimat written confirmation (Respimat WC) is an official document issued by a regulatory agency to a Respimat manufacturer, verifying that the manufacturing facility of a Respimat active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Respimat APIs or Respimat finished pharmaceutical products to another nation, regulatory agencies frequently require a Respimat WC (written confirmation) as part of the regulatory process.
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