01 1M/s. Cadila Pharmaceuticals Ltd.,
02 1M/s. Lupin Limited.,
03 1M/s. Lupin Ltd
01 1Ethambutol HCL (EP/BP/USP)
02 1Ethambutol Hydrochloride USP/EP
03 1Ethambutol Hydrochloride USP/EP/BP
01 1WC-0048
02 1WC-0074Amended
03 1WC-0201
01 3India
Date of Issue : 2022-09-01
Valid Till : 2025-07-02
Written Confirmation Number : WC-0074Amended
Address of the Firm : 294, GIDC Estate, Ankleshwar-393 002, Bharuch, Gujarat, India
Ethambutol Hydrochloride USP/EP
Date of Issue : 2022-09-30
Valid Till : 2025-09-10
Written Confirmation Number : WC-0201
Address of the Firm : T-142, MIDC, Tarapur, Vil: Boisar, Dist: Thane-401 506, Maharashtra State
Ethambutol Hydrochloride USP/EP/BP
Date of Issue : 2019-08-01
Valid Till : 2022-07-31
Written Confirmation Number : WC-0048
Address of the Firm : 124, GIDC Estate, Ankleshwar-393 002, Gujarat
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PharmaCompass offers a list of Ethambutol Dihydrochloride 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 Ethambutol Dihydrochloride manufacturer or Ethambutol Dihydrochloride supplier for your needs.
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A C10H24N2O2.2HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C10H24N2O2.2HCl, including repackagers and relabelers. The FDA regulates C10H24N2O2.2HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C10H24N2O2.2HCl 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 C10H24N2O2.2HCl supplier is an individual or a company that provides C10H24N2O2.2HCl active pharmaceutical ingredient (API) or C10H24N2O2.2HCl finished formulations upon request. The C10H24N2O2.2HCl suppliers may include C10H24N2O2.2HCl API manufacturers, exporters, distributors and traders.
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A C10H24N2O2.2HCl written confirmation (C10H24N2O2.2HCl WC) is an official document issued by a regulatory agency to a C10H24N2O2.2HCl manufacturer, verifying that the manufacturing facility of a C10H24N2O2.2HCl active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting C10H24N2O2.2HCl APIs or C10H24N2O2.2HCl finished pharmaceutical products to another nation, regulatory agencies frequently require a C10H24N2O2.2HCl WC (written confirmation) as part of the regulatory process.
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