01 1M/s RPG Life Sciences Limited
01 1Propantheline Bromide BP/EP/USP
01 1WC-0056
01 1India
Propantheline Bromide BP/EP/USP
Date of Issue : 2022-06-03
Valid Till : 2025-07-28
Written Confirmation Number : WC-0056
Address of the Firm : Plot No.2702, A, GIDC, Estate Ankleshwar, Dist Bharuch, Gujarat
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PharmaCompass offers a list of Propantheline Bromide 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 Propantheline Bromide manufacturer or Propantheline Bromide supplier for your needs.
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PharmaCompass also assists you with knowing the Propantheline Bromide API Price utilized in the formulation of products. Propantheline Bromide API Price is not always fixed or binding as the Propantheline Bromide Price is obtained through a variety of data sources. The Propantheline Bromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ketaman manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ketaman, including repackagers and relabelers. The FDA regulates Ketaman manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ketaman 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 Ketaman manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ketaman supplier is an individual or a company that provides Ketaman active pharmaceutical ingredient (API) or Ketaman finished formulations upon request. The Ketaman suppliers may include Ketaman API manufacturers, exporters, distributors and traders.
click here to find a list of Ketaman suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ketaman written confirmation (Ketaman WC) is an official document issued by a regulatory agency to a Ketaman manufacturer, verifying that the manufacturing facility of a Ketaman active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ketaman APIs or Ketaman finished pharmaceutical products to another nation, regulatory agencies frequently require a Ketaman WC (written confirmation) as part of the regulatory process.
click here to find a list of Ketaman suppliers with Written Confirmation (WC) on PharmaCompass.
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