EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1Sanofi Winthrop Industrie
02 1Apitoria Pharma Private Limited Unit-I
03 1삼진제약(주)
01 1Aging Life Science Co., Ltd.
02 1Sanofi-Aventis Korea Co., Ltd.
03 1삼진제약(주)
01 3Amisulpiride
01 1France
02 1India
03 1South Korea
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registrant Name : Sanofi-Aventis Korea Co., Ltd.
Registration Date : 2022-09-22
Registration Number : 20220922-209-J-1388
Manufacturer Name : Sanofi Winthrop Industrie
Manufacturer Address : 45 Chemin De Météline, Sisteron, 04200, France
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2021-05-03
Registration Number : 20210503-209-J-965
Manufacturer Name : Apitoria Pharma Private Limi...
Manufacturer Address : Unit-I, Sy.No. 379, 385, 386, 388 - 396, Borpatla Village, Hatnoora Mandal, Sangaredd...
Registrant Name : 삼진제약(주)
Registration Date : 2023-03-15
Registration Number : 20230315-209-J-1460
Manufacturer Name : 삼진제약(주)
Manufacturer Address : 156 Osong Life 6-ro, Osong-eup, Heungdeok-gu, Cheongju-si, Chungcheongbuk-do
70
PharmaCompass offers a list of Amisulpride 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 Amisulpride manufacturer or Amisulpride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Amisulpride manufacturer or Amisulpride supplier.
PharmaCompass also assists you with knowing the Amisulpride API Price utilized in the formulation of products. Amisulpride API Price is not always fixed or binding as the Amisulpride Price is obtained through a variety of data sources. The Amisulpride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Deniban manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Deniban, including repackagers and relabelers. The FDA regulates Deniban manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Deniban 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 Deniban manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Deniban supplier is an individual or a company that provides Deniban active pharmaceutical ingredient (API) or Deniban finished formulations upon request. The Deniban suppliers may include Deniban API manufacturers, exporters, distributors and traders.
click here to find a list of Deniban 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 Deniban Drug Master File in Korea (Deniban KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Deniban. The MFDS reviews the Deniban KDMF as part of the drug registration process and uses the information provided in the Deniban KDMF to evaluate the safety and efficacy of the drug.
After submitting a Deniban 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 Deniban API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Deniban suppliers with KDMF on PharmaCompass.
We have 3 companies offering Deniban
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