01 1Beijing Jincheng Taier Pharmaceutical Co. Ltd.
02 1Wockhardt Limited
01 1Masung LS Co., Ltd.
02 1Samoh Pharmaceutical Co., Ltd.
01 2Pidotti mode
01 1China
02 1India
Registrant Name : Masung LS Co., Ltd.
Registration Date : 2022-05-24
Registration Number : 20220524-211-J-1303
Manufacturer Name : Beijing Jincheng Taier Pharm...
Manufacturer Address : The eastern longitute 5 Road, Northern latitude 2 Road of Beijing Pharmaceutical Indu...
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2021-12-15
Registration Number : 20211215-211-J-1179
Manufacturer Name : Wockhardt Limited
Manufacturer Address : Plot No. 138, Ankleshwar-393 002, Dist. Bharuch, Gujarat State, India
A Pidotimod manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pidotimod, including repackagers and relabelers. The FDA regulates Pidotimod manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pidotimod 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 Pidotimod manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pidotimod supplier is an individual or a company that provides Pidotimod active pharmaceutical ingredient (API) or Pidotimod finished formulations upon request. The Pidotimod suppliers may include Pidotimod API manufacturers, exporters, distributors and traders.
click here to find a list of Pidotimod 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 Pidotimod Drug Master File in Korea (Pidotimod KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Pidotimod. The MFDS reviews the Pidotimod KDMF as part of the drug registration process and uses the information provided in the Pidotimod KDMF to evaluate the safety and efficacy of the drug.
After submitting a Pidotimod 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 Pidotimod API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Pidotimod suppliers with KDMF on PharmaCompass.
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