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 : CEP 2016-060 - Rev 01
Status : Valid
Issue Date : 2025-04-08
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ethambutol Dihydrochloride manufacturer or Ethambutol Dihydrochloride supplier.
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 E1011 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E1011, including repackagers and relabelers. The FDA regulates E1011 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E1011 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 E1011 supplier is an individual or a company that provides E1011 active pharmaceutical ingredient (API) or E1011 finished formulations upon request. The E1011 suppliers may include E1011 API manufacturers, exporters, distributors and traders.
click here to find a list of E1011 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A E1011 CEP of the European Pharmacopoeia monograph is often referred to as a E1011 Certificate of Suitability (COS). The purpose of a E1011 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of E1011 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of E1011 to their clients by showing that a E1011 CEP has been issued for it. The manufacturer submits a E1011 CEP (COS) as part of the market authorization procedure, and it takes on the role of a E1011 CEP holder for the record. Additionally, the data presented in the E1011 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the E1011 DMF.
A E1011 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. E1011 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 E1011 suppliers with CEP (COS) on PharmaCompass.
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