01 1LUPIN LIMITED Mumbai IN
02 2MICRO LABS LIMITED Bengaluru IN
01 2Ethambutol hydrochloride
02 1Ethambutol hydrochloride, Process-II
01 3India
01 3Valid
Certificate Number : R1-CEP 2000-019 - Rev 06
Status : Valid
Issue Date : 2021-03-18
Type : Chemical
Substance Number : 553
Certificate Number : CEP 2016-060 - Rev 01
Status : Valid
Issue Date : 2025-04-08
Type : Chemical
Substance Number : 553
Ethambutol Hydrochloride, Process-II
Certificate Number : CEP 2023-224 - Rev 00
Status : Valid
Issue Date : 2023-09-07
Type : Chemical
Substance Number : 553
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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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PharmaCompass also assists you with knowing the Ethambutol Dihydrochloride API Price utilized in the formulation of products. Ethambutol Dihydrochloride API Price is not always fixed or binding as the Ethambutol Dihydrochloride Price is obtained through a variety of data sources. The Ethambutol Dihydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
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 CEP of the European Pharmacopoeia monograph is often referred to as a C10H24N2O2.2HCl Certificate of Suitability (COS). The purpose of a C10H24N2O2.2HCl CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of C10H24N2O2.2HCl EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of C10H24N2O2.2HCl to their clients by showing that a C10H24N2O2.2HCl CEP has been issued for it. The manufacturer submits a C10H24N2O2.2HCl CEP (COS) as part of the market authorization procedure, and it takes on the role of a C10H24N2O2.2HCl CEP holder for the record. Additionally, the data presented in the C10H24N2O2.2HCl CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the C10H24N2O2.2HCl DMF.
A C10H24N2O2.2HCl CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. C10H24N2O2.2HCl CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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