Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
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01 1EGIS PHARMACEUTICALS PRIVATE LIMITED COMPANY
02 1SANOFI WINTHROP INDUSTRIE
03 1Shanghai Med-Pharma Factory Fifteen Co. Ltd.
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01 1Chlorpromazine Hydrochloride
02 2Chlorpromazine hydrochloride
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01 1France
02 1Hungary
03 1Blank
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Registration Number : 304MF10157
Registrant's Address : H-1106 BUDAPEST KERESZTURI UT 30-38 HUNGARY
Initial Date of Registration : 2022-12-15
Latest Date of Registration : 2022-12-15
Registration Number : 222MF10096
Registrant's Address : 82 Avenue Raspail 94250 Gentilly France
Initial Date of Registration : 2010-03-17
Latest Date of Registration : 2013-08-28
Registration Number : 219MF10261
Registrant's Address : 1440 Bei Di Road. Shanghai, China
Initial Date of Registration : 2007-08-06
Latest Date of Registration : 2007-08-06
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A 2-Chlorophenothiazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 2-Chlorophenothiazine, including repackagers and relabelers. The FDA regulates 2-Chlorophenothiazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 2-Chlorophenothiazine 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 2-Chlorophenothiazine supplier is an individual or a company that provides 2-Chlorophenothiazine active pharmaceutical ingredient (API) or 2-Chlorophenothiazine finished formulations upon request. The 2-Chlorophenothiazine suppliers may include 2-Chlorophenothiazine API manufacturers, exporters, distributors and traders.
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The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The 2-Chlorophenothiazine Drug Master File in Japan (2-Chlorophenothiazine JDMF) empowers 2-Chlorophenothiazine API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the 2-Chlorophenothiazine JDMF during the approval evaluation for pharmaceutical products. At the time of 2-Chlorophenothiazine JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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