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01 1M/s. Natco Pharma Ltd,
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01 1Trihexyphenidyl Hydrochloride (USP/Ph.Eur.)
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01 1WC-0014
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01 1India
Trihexyphenidyl Hydrochloride (USP/Ph.Eur.)
Date of Issue : 2019-06-26
Valid Till : 2022-06-25
Written Confirmation Number : WC-0014
Address of the Firm : Mekaguda (V) kothur (M) Mahabood nagar Dist, Telangana State India
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PharmaCompass offers a list of Benzhexol 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 Benzhexol hydrochloride manufacturer or Benzhexol hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Benzhexol hydrochloride API Price utilized in the formulation of products. Benzhexol hydrochloride API Price is not always fixed or binding as the Benzhexol hydrochloride Price is obtained through a variety of data sources. The Benzhexol hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Triesifenidile manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triesifenidile, including repackagers and relabelers. The FDA regulates Triesifenidile manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triesifenidile 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 Triesifenidile supplier is an individual or a company that provides Triesifenidile active pharmaceutical ingredient (API) or Triesifenidile finished formulations upon request. The Triesifenidile suppliers may include Triesifenidile API manufacturers, exporters, distributors and traders.
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A Triesifenidile written confirmation (Triesifenidile WC) is an official document issued by a regulatory agency to a Triesifenidile manufacturer, verifying that the manufacturing facility of a Triesifenidile active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Triesifenidile APIs or Triesifenidile finished pharmaceutical products to another nation, regulatory agencies frequently require a Triesifenidile WC (written confirmation) as part of the regulatory process.
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