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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Selegiline Hydrochloride manufacturer or Selegiline Hydrochloride supplier.
PharmaCompass also assists you with knowing the Selegiline Hydrochloride API Price utilized in the formulation of products. Selegiline Hydrochloride API Price is not always fixed or binding as the Selegiline Hydrochloride Price is obtained through a variety of data sources. The Selegiline Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Plurimen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Plurimen, including repackagers and relabelers. The FDA regulates Plurimen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Plurimen 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 Plurimen supplier is an individual or a company that provides Plurimen active pharmaceutical ingredient (API) or Plurimen finished formulations upon request. The Plurimen suppliers may include Plurimen API manufacturers, exporters, distributors and traders.
click here to find a list of Plurimen suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Plurimen written confirmation (Plurimen WC) is an official document issued by a regulatory agency to a Plurimen manufacturer, verifying that the manufacturing facility of a Plurimen active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Plurimen APIs or Plurimen finished pharmaceutical products to another nation, regulatory agencies frequently require a Plurimen WC (written confirmation) as part of the regulatory process.
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