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 Ipratropium Bromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ipratropium Bromide, including repackagers and relabelers. The FDA regulates Ipratropium Bromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ipratropium Bromide 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 Ipratropium Bromide supplier is an individual or a company that provides Ipratropium Bromide active pharmaceutical ingredient (API) or Ipratropium Bromide finished formulations upon request. The Ipratropium Bromide suppliers may include Ipratropium Bromide API manufacturers, exporters, distributors and traders.
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A Ipratropium Bromide written confirmation (Ipratropium Bromide WC) is an official document issued by a regulatory agency to a Ipratropium Bromide manufacturer, verifying that the manufacturing facility of a Ipratropium Bromide active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ipratropium Bromide APIs or Ipratropium Bromide finished pharmaceutical products to another nation, regulatory agencies frequently require a Ipratropium Bromide WC (written confirmation) as part of the regulatory process.
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