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....
90
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Levalbuterol Hydrochloride manufacturer or Levalbuterol Hydrochloride supplier.
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 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levalbuterol, including repackagers and relabelers. The FDA regulates Levalbuterol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levalbuterol API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Levalbuterol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levalbuterol supplier is an individual or a company that provides Levalbuterol active pharmaceutical ingredient (API) or Levalbuterol finished formulations upon request. The Levalbuterol suppliers may include Levalbuterol API manufacturers, exporters, distributors and traders.
click here to find a list of Levalbuterol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Levalbuterol written confirmation (Levalbuterol WC) is an official document issued by a regulatory agency to a Levalbuterol manufacturer, verifying that the manufacturing facility of a Levalbuterol active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Levalbuterol APIs or Levalbuterol finished pharmaceutical products to another nation, regulatory agencies frequently require a Levalbuterol WC (written confirmation) as part of the regulatory process.
click here to find a list of Levalbuterol suppliers with Written Confirmation (WC) on PharmaCompass.
We have 2 companies offering Levalbuterol
Get in contact with the supplier of your choice:
