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01 1M/s Quantum Drugs and Chemicals
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01 1Chlorpropamide BP/EP/USP
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01 1WC-0332n
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01 1India
Date of Issue : 2022-01-20
Valid Till : 2024-09-30
Written Confirmation Number : WC-0332n
Address of the Firm : C-21, SIPCOT Industrial Complex, Manamadurai - 630 606, Sivaganga District, Mana...
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PharmaCompass offers a list of Chlorpropamide 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 Chlorpropamide manufacturer or Chlorpropamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlorpropamide manufacturer or Chlorpropamide supplier.
PharmaCompass also assists you with knowing the Chlorpropamide API Price utilized in the formulation of products. Chlorpropamide API Price is not always fixed or binding as the Chlorpropamide Price is obtained through a variety of data sources. The Chlorpropamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A dia benese manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of dia benese, including repackagers and relabelers. The FDA regulates dia benese manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. dia benese 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 dia benese supplier is an individual or a company that provides dia benese active pharmaceutical ingredient (API) or dia benese finished formulations upon request. The dia benese suppliers may include dia benese API manufacturers, exporters, distributors and traders.
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A dia benese written confirmation (dia benese WC) is an official document issued by a regulatory agency to a dia benese manufacturer, verifying that the manufacturing facility of a dia benese active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting dia benese APIs or dia benese finished pharmaceutical products to another nation, regulatory agencies frequently require a dia benese WC (written confirmation) as part of the regulatory process.
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