01 1M/s. Hemmo Pharmaceuticals Pvt. Ltd
01 1Tetracosactide (Ph. Eur.)
01 1WC-0237
01 1India
Date of Issue : 2019-09-03
Valid Till : 2022-09-02
Written Confirmation Number : WC-0237
Address of the Firm : C-43, MIDC, TTC Industrial Area, Turbhe, Off Thane Belapur Road, Dist: Thane Mah...
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PharmaCompass offers a list of Tetracosactide 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 Tetracosactide manufacturer or Tetracosactide supplier for your needs.
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PharmaCompass also assists you with knowing the Tetracosactide API Price utilized in the formulation of products. Tetracosactide API Price is not always fixed or binding as the Tetracosactide Price is obtained through a variety of data sources. The Tetracosactide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cosyntropin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cosyntropin, including repackagers and relabelers. The FDA regulates Cosyntropin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cosyntropin 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 Cosyntropin supplier is an individual or a company that provides Cosyntropin active pharmaceutical ingredient (API) or Cosyntropin finished formulations upon request. The Cosyntropin suppliers may include Cosyntropin API manufacturers, exporters, distributors and traders.
click here to find a list of Cosyntropin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cosyntropin written confirmation (Cosyntropin WC) is an official document issued by a regulatory agency to a Cosyntropin manufacturer, verifying that the manufacturing facility of a Cosyntropin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Cosyntropin APIs or Cosyntropin finished pharmaceutical products to another nation, regulatory agencies frequently require a Cosyntropin WC (written confirmation) as part of the regulatory process.
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