01 1M/s. Embio Ltd.,
01 1Selegiline Hydrochloride USP/BP/EP
01 1WC-0046
01 1India
Selegiline Hydrochloride USP/BP/EP
Date of Issue : 2022-09-01
Valid Till : 2025-07-28
Written Confirmation Number : WC-0046
Address of the Firm : Plot No. E-21, E-22/1, MIDC, Mahad, Dist. Raigad-402 309, Maharashtra
61
PharmaCompass offers a list of Selegiline 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 Selegiline Hydrochloride manufacturer or Selegiline Hydrochloride supplier for your needs.
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A Zelapar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zelapar, including repackagers and relabelers. The FDA regulates Zelapar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zelapar 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 Zelapar supplier is an individual or a company that provides Zelapar active pharmaceutical ingredient (API) or Zelapar finished formulations upon request. The Zelapar suppliers may include Zelapar API manufacturers, exporters, distributors and traders.
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A Zelapar written confirmation (Zelapar WC) is an official document issued by a regulatory agency to a Zelapar manufacturer, verifying that the manufacturing facility of a Zelapar active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Zelapar APIs or Zelapar finished pharmaceutical products to another nation, regulatory agencies frequently require a Zelapar WC (written confirmation) as part of the regulatory process.
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