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. Aarti Pharmalabs Limited
03 1M/s. Neuland Laboratories Ltd
04 1M/s Melody Healthcare Pvt Ltd
05 1M/s. Cipla Ltd
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
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Date of Issue : 2023-01-06
Valid Till : 2025-07-29
Written Confirmation Number : WC-0099
Address of the Firm : Plot No. E-50, 50/1 and 59/1, Unit — IV, MIDC, Tarapur — 401506, Taluka: Pal...
Neuland Laboratories- A dedicated 100% API provider.
Date of Issue : 2022-07-28
Valid Till : 2025-06-16
Written Confirmation Number : WC-0036
Address of the Firm : Unit-1, Sy. No. 347, 473, 474, 490/2, Bonthapally Village, Veerabhadraswamy, Tem...
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A COMBIVENT-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of COMBIVENT-1, including repackagers and relabelers. The FDA regulates COMBIVENT-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. COMBIVENT-1 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 COMBIVENT-1 supplier is an individual or a company that provides COMBIVENT-1 active pharmaceutical ingredient (API) or COMBIVENT-1 finished formulations upon request. The COMBIVENT-1 suppliers may include COMBIVENT-1 API manufacturers, exporters, distributors and traders.
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A COMBIVENT-1 written confirmation (COMBIVENT-1 WC) is an official document issued by a regulatory agency to a COMBIVENT-1 manufacturer, verifying that the manufacturing facility of a COMBIVENT-1 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting COMBIVENT-1 APIs or COMBIVENT-1 finished pharmaceutical products to another nation, regulatory agencies frequently require a COMBIVENT-1 WC (written confirmation) as part of the regulatory process.
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