Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1M/s Aarti Pharmalabs limited
01 1Bambuterol Hydrochloride BP/Ph. Eur
01 1WC-0295
01 1India
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Bambuterol Hydrochloride BP/Ph. Eur
Date of Issue : 2024-05-20
Valid Till : 2027-05-19
Written Confirmation Number : WC-0295
Address of the Firm : D-53, PHASE II, KALYAN SHILL ROAD, DOMBIVLI (E.), DOMBIVLI - 421204, Taluka: Dom...
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PharmaCompass offers a list of Bambuterol 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 Bambuterol Hydrochloride manufacturer or Bambuterol Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Bambuterol Hydrochloride API Price utilized in the formulation of products. Bambuterol Hydrochloride API Price is not always fixed or binding as the Bambuterol Hydrochloride Price is obtained through a variety of data sources. The Bambuterol Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxeol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxeol, including repackagers and relabelers. The FDA regulates Oxeol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxeol 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 Oxeol supplier is an individual or a company that provides Oxeol active pharmaceutical ingredient (API) or Oxeol finished formulations upon request. The Oxeol suppliers may include Oxeol API manufacturers, exporters, distributors and traders.
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A Oxeol written confirmation (Oxeol WC) is an official document issued by a regulatory agency to a Oxeol manufacturer, verifying that the manufacturing facility of a Oxeol active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Oxeol APIs or Oxeol finished pharmaceutical products to another nation, regulatory agencies frequently require a Oxeol WC (written confirmation) as part of the regulatory process.
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