01 1Boehringer Ingelheim Pharma GmbH & Co. KG Ingelheim Am Rhein DE
02 1C-SQUARED PHARMA LIMITED Cork IE
01 2Homatropine Hydrobromide
01 1Germany
02 1Ireland
01 1Valid
02 1Withdrawn by Holder
Certificate Number : R1-CEP 2001-176 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2007-11-15
Type : Chemical
Substance Number : 500
Certificate Number : CEP 2020-115 - Rev 02
Status : Valid
Issue Date : 2024-08-14
Type : Chemical
Substance Number : 500
A Homatropine Hydrobromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Homatropine Hydrobromide, including repackagers and relabelers. The FDA regulates Homatropine Hydrobromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Homatropine Hydrobromide 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 Homatropine Hydrobromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Homatropine Hydrobromide supplier is an individual or a company that provides Homatropine Hydrobromide active pharmaceutical ingredient (API) or Homatropine Hydrobromide finished formulations upon request. The Homatropine Hydrobromide suppliers may include Homatropine Hydrobromide API manufacturers, exporters, distributors and traders.
click here to find a list of Homatropine Hydrobromide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Homatropine Hydrobromide CEP of the European Pharmacopoeia monograph is often referred to as a Homatropine Hydrobromide Certificate of Suitability (COS). The purpose of a Homatropine Hydrobromide CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Homatropine Hydrobromide EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Homatropine Hydrobromide to their clients by showing that a Homatropine Hydrobromide CEP has been issued for it. The manufacturer submits a Homatropine Hydrobromide CEP (COS) as part of the market authorization procedure, and it takes on the role of a Homatropine Hydrobromide CEP holder for the record. Additionally, the data presented in the Homatropine Hydrobromide CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Homatropine Hydrobromide DMF.
A Homatropine Hydrobromide CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Homatropine Hydrobromide 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 Homatropine Hydrobromide suppliers with CEP (COS) on PharmaCompass.
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