01 1M/s Orex Pharma Pvt Ltd
01 1Bromhexine Hydrochloride EP/BP
01 1WC-0534N
01 1India
Bromhexine Hydrochloride EP/BP
Date of Issue : 2022-08-31
Valid Till : 2025-08-30
Written Confirmation Number : WC-0534N
Address of the Firm : B-5, Phase 1, MIDC Dombivli, Dombivali I.A. - 421203, Taluka : Dombivali City, D...
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PharmaCompass offers a list of Bromhexine 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 Bromhexine Hydrochloride manufacturer or Bromhexine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Bromhexine Hydrochloride API Price utilized in the formulation of products. Bromhexine Hydrochloride API Price is not always fixed or binding as the Bromhexine Hydrochloride Price is obtained through a variety of data sources. The Bromhexine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bisolvon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bisolvon, including repackagers and relabelers. The FDA regulates Bisolvon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bisolvon 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 Bisolvon supplier is an individual or a company that provides Bisolvon active pharmaceutical ingredient (API) or Bisolvon finished formulations upon request. The Bisolvon suppliers may include Bisolvon API manufacturers, exporters, distributors and traders.
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A Bisolvon written confirmation (Bisolvon WC) is an official document issued by a regulatory agency to a Bisolvon manufacturer, verifying that the manufacturing facility of a Bisolvon active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Bisolvon APIs or Bisolvon finished pharmaceutical products to another nation, regulatory agencies frequently require a Bisolvon WC (written confirmation) as part of the regulatory process.
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