TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
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01 1TAPI CZECH INDUSTRIES S.R.O. Opava CZ
02 1Boehringer Ingelheim Pharma GmbH & Co. KG Ingelheim Am Rhein DE
03 1CURIA ITALY S.R.L. Rozzano, Milano IT
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01 3Dihydroergotamine mesilate
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01 1Germany
02 1Israel
03 1U.S.A
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01 2Valid
02 1Withdrawn by Holder
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : CEP 2005-107 - Rev 03
Status : Valid
Issue Date : 2025-02-28
Type : Chemical
Substance Number : 551
Certificate Number : R1-CEP 2001-268 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2015-11-03
Type : Chemical
Substance Number : 551
Certificate Number : R1-CEP 2000-183 - Rev 08
Status : Valid
Issue Date : 2023-03-08
Type : Chemical
Substance Number : 551
44
PharmaCompass offers a list of Dihydroergotamine Mesylate 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 Dihydroergotamine Mesylate manufacturer or Dihydroergotamine Mesylate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dihydroergotamine Mesylate manufacturer or Dihydroergotamine Mesylate supplier.
PharmaCompass also assists you with knowing the Dihydroergotamine Mesylate API Price utilized in the formulation of products. Dihydroergotamine Mesylate API Price is not always fixed or binding as the Dihydroergotamine Mesylate Price is obtained through a variety of data sources. The Dihydroergotamine Mesylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DHE 45 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DHE 45, including repackagers and relabelers. The FDA regulates DHE 45 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DHE 45 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 DHE 45 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DHE 45 supplier is an individual or a company that provides DHE 45 active pharmaceutical ingredient (API) or DHE 45 finished formulations upon request. The DHE 45 suppliers may include DHE 45 API manufacturers, exporters, distributors and traders.
click here to find a list of DHE 45 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DHE 45 CEP of the European Pharmacopoeia monograph is often referred to as a DHE 45 Certificate of Suitability (COS). The purpose of a DHE 45 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DHE 45 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DHE 45 to their clients by showing that a DHE 45 CEP has been issued for it. The manufacturer submits a DHE 45 CEP (COS) as part of the market authorization procedure, and it takes on the role of a DHE 45 CEP holder for the record. Additionally, the data presented in the DHE 45 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DHE 45 DMF.
A DHE 45 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DHE 45 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 DHE 45 suppliers with CEP (COS) on PharmaCompass.
We have 3 companies offering DHE 45
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