01 1Dynamit Nobel GmbH, Explosivstoff- und Systemtechnik Leverkusen DE
02 1ONY, INC. Amherst US
01 1Calf Lung Surfactant Extract
02 1Glyceryl trinitrate solution
01 1Germany
02 1U.S.A
01 2Valid
Certificate Number : CEP 2003-185 - Rev 02
Status : Valid
Issue Date : 2025-03-11
Type : Chemical
Substance Number : 1331
Certificate Number : R1-CEP 2008-285 - Rev 00
Status : Valid
Issue Date : 2014-05-19
Type : TSE
Substance Number :
12
PharmaCompass offers a list of Nitroglycerin 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 Nitroglycerin manufacturer or Nitroglycerin supplier for your needs.
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A Nitromack Retard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nitromack Retard, including repackagers and relabelers. The FDA regulates Nitromack Retard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nitromack Retard 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 Nitromack Retard supplier is an individual or a company that provides Nitromack Retard active pharmaceutical ingredient (API) or Nitromack Retard finished formulations upon request. The Nitromack Retard suppliers may include Nitromack Retard API manufacturers, exporters, distributors and traders.
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A Nitromack Retard CEP of the European Pharmacopoeia monograph is often referred to as a Nitromack Retard Certificate of Suitability (COS). The purpose of a Nitromack Retard CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Nitromack Retard EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Nitromack Retard to their clients by showing that a Nitromack Retard CEP has been issued for it. The manufacturer submits a Nitromack Retard CEP (COS) as part of the market authorization procedure, and it takes on the role of a Nitromack Retard CEP holder for the record. Additionally, the data presented in the Nitromack Retard CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Nitromack Retard DMF.
A Nitromack Retard CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Nitromack Retard 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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