01 1M/s Embio Limited
01 1Ephedrine Sulfate USP
01 1WC-0046
01 1India
Date of Issue : 2022-01-09
Valid Till : 2025-07-28
Written Confirmation Number : WC-0046
Address of the Firm : E-21, MIDC, Indt. Estate, Mahad-402 309, Taluka: Mahad, District: Raigad, Mahara...
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PharmaCompass offers a list of Ephedrine Sulfate 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 Ephedrine Sulfate manufacturer or Ephedrine Sulfate supplier for your needs.
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PharmaCompass also assists you with knowing the Ephedrine Sulfate API Price utilized in the formulation of products. Ephedrine Sulfate API Price is not always fixed or binding as the Ephedrine Sulfate Price is obtained through a variety of data sources. The Ephedrine Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A E 3250 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E 3250, including repackagers and relabelers. The FDA regulates E 3250 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E 3250 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 E 3250 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A E 3250 supplier is an individual or a company that provides E 3250 active pharmaceutical ingredient (API) or E 3250 finished formulations upon request. The E 3250 suppliers may include E 3250 API manufacturers, exporters, distributors and traders.
click here to find a list of E 3250 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A E 3250 written confirmation (E 3250 WC) is an official document issued by a regulatory agency to a E 3250 manufacturer, verifying that the manufacturing facility of a E 3250 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting E 3250 APIs or E 3250 finished pharmaceutical products to another nation, regulatory agencies frequently require a E 3250 WC (written confirmation) as part of the regulatory process.
click here to find a list of E 3250 suppliers with Written Confirmation (WC) on PharmaCompass.
