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 Coral Drugs Pvt Ltd
03 1M/s. Aarti Pharmalabs Limited
04 1Hubei Gedian Humanwell Pharmaceutical Co., Ltd
05 1M/s. Avik Pharmaceutical Limited
06 1M/s. Sun Pharmaceuticals Ltd.
07 1M/s.Cipla Limited
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
Coral's API range includes Corticosteroids, Antihistamines. Hormones and Antineoplastics.
Date of Issue : 2022-09-16
Valid Till : 2025-07-05
Written Confirmation Number : WC-0009
Address of the Firm : Plot No. 55, 56 & 57, HSIIDC Industrial Estate, Murthal, Sonipat 131029, Haryana
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...
A Budesonide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Budesonide, including repackagers and relabelers. The FDA regulates Budesonide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Budesonide 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 Budesonide supplier is an individual or a company that provides Budesonide active pharmaceutical ingredient (API) or Budesonide finished formulations upon request. The Budesonide suppliers may include Budesonide API manufacturers, exporters, distributors and traders.
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A Budesonide written confirmation (Budesonide WC) is an official document issued by a regulatory agency to a Budesonide manufacturer, verifying that the manufacturing facility of a Budesonide active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Budesonide APIs or Budesonide finished pharmaceutical products to another nation, regulatory agencies frequently require a Budesonide WC (written confirmation) as part of the regulatory process.
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