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.
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PharmaCompass offers a list of Sucralfate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Sucralfate manufacturer or Sucralfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sucralfate manufacturer or Sucralfate supplier.
PharmaCompass also assists you with knowing the Sucralfate API Price utilized in the formulation of products. Sucralfate API Price is not always fixed or binding as the Sucralfate Price is obtained through a variety of data sources. The Sucralfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ulsanic manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ulsanic, including repackagers and relabelers. The FDA regulates Ulsanic manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ulsanic 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 Ulsanic manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ulsanic supplier is an individual or a company that provides Ulsanic active pharmaceutical ingredient (API) or Ulsanic finished formulations upon request. The Ulsanic suppliers may include Ulsanic API manufacturers, exporters, distributors and traders.
click here to find a list of Ulsanic 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 Ulsanic Drug Master File in Korea (Ulsanic KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ulsanic. The MFDS reviews the Ulsanic KDMF as part of the drug registration process and uses the information provided in the Ulsanic KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ulsanic 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 Ulsanic API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Ulsanic suppliers with KDMF on PharmaCompass.
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