01 1Bidachem S.p.A. Fornovo San Giovanni IT
02 2Boehringer Ingelheim Pharma GmbH & Co. KG Ingelheim Am Rhein DE
01 2Orciprenaline sulfate
02 1Orciprenaline sulfate, Micronised (particle size 5 µm)
01 2Germany
02 1Italy
01 1Expired
02 1Valid
03 1Withdrawn by Holder
Certificate Number : R1-CEP 2004-217 - Rev 00
Status : Valid
Issue Date : 2012-03-07
Type : Chemical
Substance Number : 1033
Certificate Number : R0-CEP 2001-235 - Rev 01
Status : Expired
Issue Date : 2004-10-13
Type : Chemical
Substance Number : 1033
Orciprenaline Sulfate, Micronised (particle Size...
Certificate Number : R0-CEP 2001-236 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2004-10-13
Type : Chemical
Substance Number : 1033
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PharmaCompass offers a list of Metaproterenol Hemisulfate 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 Metaproterenol Hemisulfate manufacturer or Metaproterenol Hemisulfate supplier for your needs.
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A Alupent manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alupent, including repackagers and relabelers. The FDA regulates Alupent manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alupent 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 Alupent supplier is an individual or a company that provides Alupent active pharmaceutical ingredient (API) or Alupent finished formulations upon request. The Alupent suppliers may include Alupent API manufacturers, exporters, distributors and traders.
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A Alupent CEP of the European Pharmacopoeia monograph is often referred to as a Alupent Certificate of Suitability (COS). The purpose of a Alupent CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Alupent EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Alupent to their clients by showing that a Alupent CEP has been issued for it. The manufacturer submits a Alupent CEP (COS) as part of the market authorization procedure, and it takes on the role of a Alupent CEP holder for the record. Additionally, the data presented in the Alupent CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Alupent DMF.
A Alupent CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Alupent 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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