Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.

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01 1EGIS Pharmaceuticals PLC Budapest HU
02 2ZHEJIANG CHIRAL MEDICINE CHEMICALS CO., LTD. Hangzhou CN
03 1ZHEJIANG WILD WIND PHARMACEUTICAL CO., LTD. Geshan Town CN
04 1ZHEJIANG YONGTAI CHIRAL MEDICINE TECHNOLOGY CO. LTD. Taizhou CN
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01 3Methyldopa
02 1Methyldopa, Process B
03 1Methyldopa, Site Yongtai Chiral, Process A
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01 4China
02 1Hungary
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01 5Valid
Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.
Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.
Certificate Number : R1-CEP 1996-033 - Rev 07
Status : Valid
Issue Date : 2019-04-10
Type : Chemical
Substance Number : 45
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Certificate Number : R1-CEP 2018-065 - Rev 00
Status : Valid
Issue Date : 2023-06-20
Type : Chemical
Substance Number : 45

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Certificate Number : R1-CEP 2003-241 - Rev 03
Status : Valid
Issue Date : 2017-05-17
Type : Chemical
Substance Number : 45

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Certificate Number : R1-CEP 2009-120 - Rev 01
Status : Valid
Issue Date : 2018-04-18
Type : Chemical
Substance Number : 45

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Methyldopa, Site Yongtai Chiral, Process A
Certificate Number : CEP 2025-526 - Rev 00
Status : Valid
Issue Date : 2026-01-21
Type : Chemical
Substance Number : 45

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PharmaCompass offers a list of Methyldopa API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Methyldopa manufacturer or Methyldopa supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Methyldopa manufacturer or Methyldopa supplier.
A Hyperpax manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hyperpax, including repackagers and relabelers. The FDA regulates Hyperpax manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hyperpax 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 Hyperpax manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Hyperpax supplier is an individual or a company that provides Hyperpax active pharmaceutical ingredient (API) or Hyperpax finished formulations upon request. The Hyperpax suppliers may include Hyperpax API manufacturers, exporters, distributors and traders.
click here to find a list of Hyperpax suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Hyperpax CEP of the European Pharmacopoeia monograph is often referred to as a Hyperpax Certificate of Suitability (COS). The purpose of a Hyperpax CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hyperpax EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hyperpax to their clients by showing that a Hyperpax CEP has been issued for it. The manufacturer submits a Hyperpax CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hyperpax CEP holder for the record. Additionally, the data presented in the Hyperpax CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hyperpax DMF.
A Hyperpax CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hyperpax 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 Hyperpax suppliers with CEP (COS) on PharmaCompass.
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