01 1M/s. Embio Ltd.,
01 1Di-Norpseudoephedrine IH
01 1WC-0046
01 1India
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
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PharmaCompass offers a list of Phenylpropanolamine 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 Phenylpropanolamine manufacturer or Phenylpropanolamine supplier for your needs.
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PharmaCompass also assists you with knowing the Phenylpropanolamine API Price utilized in the formulation of products. Phenylpropanolamine API Price is not always fixed or binding as the Phenylpropanolamine Price is obtained through a variety of data sources. The Phenylpropanolamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dl-Norephedrine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dl-Norephedrine Hydrochloride, including repackagers and relabelers. The FDA regulates Dl-Norephedrine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dl-Norephedrine Hydrochloride 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 Dl-Norephedrine Hydrochloride supplier is an individual or a company that provides Dl-Norephedrine Hydrochloride active pharmaceutical ingredient (API) or Dl-Norephedrine Hydrochloride finished formulations upon request. The Dl-Norephedrine Hydrochloride suppliers may include Dl-Norephedrine Hydrochloride API manufacturers, exporters, distributors and traders.
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A Dl-Norephedrine Hydrochloride written confirmation (Dl-Norephedrine Hydrochloride WC) is an official document issued by a regulatory agency to a Dl-Norephedrine Hydrochloride manufacturer, verifying that the manufacturing facility of a Dl-Norephedrine Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Dl-Norephedrine Hydrochloride APIs or Dl-Norephedrine Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Dl-Norephedrine Hydrochloride WC (written confirmation) as part of the regulatory process.
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