01 1Elementis Pharma GmbH
02 3Zhejiang Haisen Pharmaceutical Co., Ltd
01 1Intro Biopharma Co., Ltd.
02 1Korea Pavise Pharmaceutical Co., Ltd.
03 1Kukjeon Pharmaceutical Co., Ltd.
04 1Sechang International Co., Ltd.
01 4sucralfate hydrate
01 3China
02 1Germany
Registrant Name : Korea Pavise Pharmaceutical Co., Ltd.
Registration Date : 2019-06-25
Registration Number : 20190625-211-J-370
Manufacturer Name : Elementis Pharma GmbH
Manufacturer Address : Giulinistr. 2 67065 Ludwigshafen Germany
Registrant Name : Intro Biopharma Co., Ltd.
Registration Date : 2019-04-03
Registration Number : 20190211-211-J-310(1)
Manufacturer Name : Zhejiang Haisen Pharmaceutic...
Manufacturer Address : Xiangtan Village, Liushi Street, Dongyang City, Zhejiang Province, China.
Registrant Name : Sechang International Co., Ltd.
Registration Date : 2019-02-11
Registration Number : 20190211-211-J-310
Manufacturer Name : Zhejiang Haisen Pharmaceutic...
Manufacturer Address : Xiangtan Village, Liushi Street, Dongyang City, Zhejiang Province, China.
Registrant Name : Kukjeon Pharmaceutical Co., Ltd.
Registration Date : 2019-04-22
Registration Number : 20190211-211-J-310(2)
Manufacturer Name : Zhejiang Haisen Pharmaceutic...
Manufacturer Address : Xiangtan Village, Liushi Street, Dongyang City, Zhejiang Province, China.
A Sucralfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sucralfate, including repackagers and relabelers. The FDA regulates Sucralfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sucralfate 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 Sucralfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sucralfate supplier is an individual or a company that provides Sucralfate active pharmaceutical ingredient (API) or Sucralfate finished formulations upon request. The Sucralfate suppliers may include Sucralfate API manufacturers, exporters, distributors and traders.
click here to find a list of Sucralfate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Sucralfate Drug Master File in Korea (Sucralfate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Sucralfate. The MFDS reviews the Sucralfate KDMF as part of the drug registration process and uses the information provided in the Sucralfate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Sucralfate 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 Sucralfate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Sucralfate suppliers with KDMF on PharmaCompass.
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