01 1M/s. Centauar Pharmacerticals Pvt. Ltd.,
01 1Propiverine Hydrochloride IH
01 1WC-0107
01 1India
Date of Issue : 2022-06-08
Valid Till : 2025-06-25
Written Confirmation Number : WC-0107
Address of the Firm : Plot No. 75/76, Chikhloli, MIDC, Ambernath (W), Dist- Thane 421501 Maharashtra ...
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PharmaCompass offers a list of Propiverine 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 Propiverine Hydrochloride manufacturer or Propiverine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Propiverine Hydrochloride manufacturer or Propiverine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Propiverine Hydrochloride API Price utilized in the formulation of products. Propiverine Hydrochloride API Price is not always fixed or binding as the Propiverine Hydrochloride Price is obtained through a variety of data sources. The Propiverine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Detrunorm manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Detrunorm, including repackagers and relabelers. The FDA regulates Detrunorm manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Detrunorm 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 Detrunorm supplier is an individual or a company that provides Detrunorm active pharmaceutical ingredient (API) or Detrunorm finished formulations upon request. The Detrunorm suppliers may include Detrunorm API manufacturers, exporters, distributors and traders.
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A Detrunorm written confirmation (Detrunorm WC) is an official document issued by a regulatory agency to a Detrunorm manufacturer, verifying that the manufacturing facility of a Detrunorm active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Detrunorm APIs or Detrunorm finished pharmaceutical products to another nation, regulatory agencies frequently require a Detrunorm WC (written confirmation) as part of the regulatory process.
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