01 Gedeon Richter Ltd Budapest HU (2)
02 JIANGSU ZENJI PHARMACEUTICALS LTD. Huai'an City CN (1)
03 Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES (1)
04 Wuxi Kaili Pharmaceutical Co., Ltd. Yixing CN (1)
01 Cimetidine (3)
02 Cimetidine, Crystallised from ethanol (1)
03 Cimetidine, Crystallized from isopropanol (1)
01 China (2)
02 Hungary (2)
03 Spain (1)
01 Expired (2)
02 Valid (2)
03 Withdrawn by EDQM Failure to CEP procedure (1)
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A MolPort-001-838-193 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-838-193, including repackagers and relabelers. The FDA regulates MolPort-001-838-193 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-838-193 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 MolPort-001-838-193 supplier is an individual or a company that provides MolPort-001-838-193 active pharmaceutical ingredient (API) or MolPort-001-838-193 finished formulations upon request. The MolPort-001-838-193 suppliers may include MolPort-001-838-193 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-838-193 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MolPort-001-838-193 CEP of the European Pharmacopoeia monograph is often referred to as a MolPort-001-838-193 Certificate of Suitability (COS). The purpose of a MolPort-001-838-193 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of MolPort-001-838-193 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of MolPort-001-838-193 to their clients by showing that a MolPort-001-838-193 CEP has been issued for it. The manufacturer submits a MolPort-001-838-193 CEP (COS) as part of the market authorization procedure, and it takes on the role of a MolPort-001-838-193 CEP holder for the record. Additionally, the data presented in the MolPort-001-838-193 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the MolPort-001-838-193 DMF.
A MolPort-001-838-193 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. MolPort-001-838-193 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 MolPort-001-838-193 suppliers with CEP (COS) on PharmaCompass.
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