Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
01 1M/s Vamsi Labs Ltd
02 1M/s CIpla Limited
03 2M/s Melody healthcare Pvt Ltd
01 1Tiotropium Bromide IH
02 1Tiotropium Bromide Monohydrate BP/Ph. Eur
03 1Tiotropium Bromide Monohydrate EP
04 1Tiotropium Bromide Monohydrate EP/BP
01 1WC-0144nA2
02 1WC-0155
03 2WC-0227n
01 4India
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, A-15, A-31, A-32 & A-33, M.I.D.C. Area, Chincholi, Solapur-413 255, Mahara...
Tiotropium Bromide Monohydrate BP/Ph. Eur
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- 4138...
Tiotropium Bromide Monohydrate EP/BP
Date of Issue : 2022-07-28
Valid Till : 2025-02-07
Written Confirmation Number : WC-0227n
Address of the Firm : Plot No. J-73, MIDC, Tarapur, Boisar, Dist-Palghar 401506, Maharashtra, India
Date of Issue : 2022-07-28
Valid Till : 2025-02-07
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 SPIRIVA RESPIMAT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SPIRIVA RESPIMAT, including repackagers and relabelers. The FDA regulates SPIRIVA RESPIMAT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SPIRIVA 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.
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A SPIRIVA RESPIMAT supplier is an individual or a company that provides SPIRIVA RESPIMAT active pharmaceutical ingredient (API) or SPIRIVA RESPIMAT finished formulations upon request. The SPIRIVA RESPIMAT suppliers may include SPIRIVA RESPIMAT API manufacturers, exporters, distributors and traders.
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A SPIRIVA RESPIMAT written confirmation (SPIRIVA RESPIMAT WC) is an official document issued by a regulatory agency to a SPIRIVA RESPIMAT manufacturer, verifying that the manufacturing facility of a SPIRIVA RESPIMAT active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting SPIRIVA RESPIMAT APIs or SPIRIVA RESPIMAT finished pharmaceutical products to another nation, regulatory agencies frequently require a SPIRIVA RESPIMAT WC (written confirmation) as part of the regulatory process.
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