01 1Hunan Jiudian Hongyang Pharmaceutical.Co.,Ltd
01 1Ace Biopharm Co., Ltd.
01 1Dioctyl sodium sulfosuccinate
01 1China
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2022-12-15
Registration Number : 20221215-211-J-1422
Manufacturer Name : Hunan Jiudian Hongyang Pharm...
Manufacturer Address : Tongguan Circular Economy Industrial base, Wangcheng Economic and Technological Devel...
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PharmaCompass offers a list of Docusate Sodium 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 Docusate Sodium manufacturer or Docusate Sodium supplier for your needs.
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A Senexon-S manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Senexon-S, including repackagers and relabelers. The FDA regulates Senexon-S manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Senexon-S 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 Senexon-S manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Senexon-S supplier is an individual or a company that provides Senexon-S active pharmaceutical ingredient (API) or Senexon-S finished formulations upon request. The Senexon-S suppliers may include Senexon-S API manufacturers, exporters, distributors and traders.
click here to find a list of Senexon-S suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Senexon-S Drug Master File in Korea (Senexon-S KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Senexon-S. The MFDS reviews the Senexon-S KDMF as part of the drug registration process and uses the information provided in the Senexon-S KDMF to evaluate the safety and efficacy of the drug.
After submitting a Senexon-S KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Senexon-S API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Senexon-S suppliers with KDMF on PharmaCompass.
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