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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PharmaCompass offers a list of Levalbuterol Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Levalbuterol Hydrochloride manufacturer or Levalbuterol Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Levalbuterol Hydrochloride API Price utilized in the formulation of products. Levalbuterol Hydrochloride API Price is not always fixed or binding as the Levalbuterol Hydrochloride Price is obtained through a variety of data sources. The Levalbuterol Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Levalbuterol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levalbuterol Hydrochloride, including repackagers and relabelers. The FDA regulates Levalbuterol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levalbuterol Hydrochloride 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 Hydrochloride supplier is an individual or a company that provides Levalbuterol Hydrochloride active pharmaceutical ingredient (API) or Levalbuterol Hydrochloride finished formulations upon request. The Levalbuterol Hydrochloride suppliers may include Levalbuterol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Levalbuterol Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Levalbuterol Hydrochloride written confirmation (Levalbuterol Hydrochloride WC) is an official document issued by a regulatory agency to a Levalbuterol Hydrochloride manufacturer, verifying that the manufacturing facility of a Levalbuterol Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Levalbuterol Hydrochloride APIs or Levalbuterol Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Levalbuterol Hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Levalbuterol Hydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.
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