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
A Selegiline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Selegiline, including repackagers and relabelers. The FDA regulates Selegiline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Selegiline API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Selegiline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Selegiline supplier is an individual or a company that provides Selegiline active pharmaceutical ingredient (API) or Selegiline finished formulations upon request. The Selegiline suppliers may include Selegiline API manufacturers, exporters, distributors and traders.
click here to find a list of Selegiline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Selegiline written confirmation (Selegiline WC) is an official document issued by a regulatory agency to a Selegiline manufacturer, verifying that the manufacturing facility of a Selegiline active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Selegiline APIs or Selegiline finished pharmaceutical products to another nation, regulatory agencies frequently require a Selegiline WC (written confirmation) as part of the regulatory process.
click here to find a list of Selegiline suppliers with Written Confirmation (WC) on PharmaCompass.
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