01 1M/s. Natco Pharma Ltd,
01 1Trihexyphenidyl Hydrochloride (USP/Ph.Eur.)
01 1WC-0014
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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A Parkopan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Parkopan, including repackagers and relabelers. The FDA regulates Parkopan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Parkopan 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 Parkopan written confirmation (Parkopan WC) is an official document issued by a regulatory agency to a Parkopan manufacturer, verifying that the manufacturing facility of a Parkopan active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Parkopan APIs or Parkopan finished pharmaceutical products to another nation, regulatory agencies frequently require a Parkopan WC (written confirmation) as part of the regulatory process.
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