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
Ethambutol Hydrochloride, Process-II
Certificate Number : CEP 2023-224 - Rev 00
Status : Valid
Issue Date : 2023-09-07
Type : Chemical
Substance Number : 553
Certificate Number : R1-CEP 2016-060 - Rev 00
Status : Valid
Issue Date : 2022-09-12
Type : Chemical
Substance Number : 553
A Ethambutol Dihydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethambutol Dihydrochloride, including repackagers and relabelers. The FDA regulates Ethambutol Dihydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethambutol Dihydrochloride 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 Ethambutol Dihydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ethambutol Dihydrochloride supplier is an individual or a company that provides Ethambutol Dihydrochloride active pharmaceutical ingredient (API) or Ethambutol Dihydrochloride finished formulations upon request. The Ethambutol Dihydrochloride suppliers may include Ethambutol Dihydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Ethambutol Dihydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ethambutol Dihydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Ethambutol Dihydrochloride Certificate of Suitability (COS). The purpose of a Ethambutol Dihydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ethambutol Dihydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ethambutol Dihydrochloride to their clients by showing that a Ethambutol Dihydrochloride CEP has been issued for it. The manufacturer submits a Ethambutol Dihydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ethambutol Dihydrochloride CEP holder for the record. Additionally, the data presented in the Ethambutol Dihydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ethambutol Dihydrochloride DMF.
A Ethambutol Dihydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ethambutol Dihydrochloride CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Ethambutol Dihydrochloride suppliers with CEP (COS) on PharmaCompass.
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