01 1Hetero Drugs Limited(Unit-I)
01 1Korea Takeda Pharmaceutical Co., Ltd.
01 1Pantoprazole hemimaxine hydrate
01 1India
Pantoprazole hemimaxine hydrate
Registrant Name : Korea Takeda Pharmaceutical Co., Ltd.
Registration Date : 2022-07-08
Registration Number : 20220708-209-J-1327
Manufacturer Name : Hetero Drugs Limited(Unit-I)
Manufacturer Address : Sy.No.213, 214 & 255, Bonthapally Village, Gummadidala Mandal Sangareddy District 502...
A Pantoprazole Magnesium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pantoprazole Magnesium, including repackagers and relabelers. The FDA regulates Pantoprazole Magnesium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pantoprazole Magnesium 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 Pantoprazole Magnesium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pantoprazole Magnesium supplier is an individual or a company that provides Pantoprazole Magnesium active pharmaceutical ingredient (API) or Pantoprazole Magnesium finished formulations upon request. The Pantoprazole Magnesium suppliers may include Pantoprazole Magnesium API manufacturers, exporters, distributors and traders.
click here to find a list of Pantoprazole Magnesium 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 Pantoprazole Magnesium Drug Master File in Korea (Pantoprazole Magnesium KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Pantoprazole Magnesium. The MFDS reviews the Pantoprazole Magnesium KDMF as part of the drug registration process and uses the information provided in the Pantoprazole Magnesium KDMF to evaluate the safety and efficacy of the drug.
After submitting a Pantoprazole Magnesium 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 Pantoprazole Magnesium API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Pantoprazole Magnesium suppliers with KDMF on PharmaCompass.
We have 1 companies offering Pantoprazole Magnesium
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?