Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1M/s. Aarti Pharmalabs Limited
02 1M/s. Sun Pharmaceuticals Ltd.
01 2Levalbuterol Hydrochloride USP
01 1WC-0099
02 1WC-0168
01 2India
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Levalbuterol Hydrochloride USP
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...
Levalbuterol Hydrochloride USP
Date of Issue : 2022-08-08
Valid Till : 2025-07-14
Written Confirmation Number : WC-0168
Address of the Firm : Plot No. 24/2, & 25, Phase -IV, GIDC, Industrial Zone, At & Post - Panoli, Dist....
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A Levalbuterol HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levalbuterol HCl, including repackagers and relabelers. The FDA regulates Levalbuterol HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levalbuterol HCl 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 Levalbuterol HCl supplier is an individual or a company that provides Levalbuterol HCl active pharmaceutical ingredient (API) or Levalbuterol HCl finished formulations upon request. The Levalbuterol HCl suppliers may include Levalbuterol HCl API manufacturers, exporters, distributors and traders.
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A Levalbuterol HCl written confirmation (Levalbuterol HCl WC) is an official document issued by a regulatory agency to a Levalbuterol HCl manufacturer, verifying that the manufacturing facility of a Levalbuterol HCl active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Levalbuterol HCl APIs or Levalbuterol HCl finished pharmaceutical products to another nation, regulatory agencies frequently require a Levalbuterol HCl WC (written confirmation) as part of the regulatory process.
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