01 2Otsuka Pharmaceutical Co., Ltd.
01 2Korea Otsuka Pharmaceutical Co., Ltd.
01 2Procaterol hydrochloride
01 2Italy
Registrant Name : Korea Otsuka Pharmaceutical Co., Ltd.
Registration Date : 2012-11-30
Registration Number : 20121130-195-I-158-01
Manufacturer Name : Otsuka Pharmaceutical Co., L...
Manufacturer Address : 224-18, Hiraishi Ebisuno, Kawauchi-cho, Tokushima-shi, Tokushima, Japan
Registrant Name : Korea Otsuka Pharmaceutical Co., Ltd.
Registration Date : 2012-11-30
Registration Number : 20121130-195-I-157-02
Manufacturer Name : Otsuka Pharmaceutical Co., L...
Manufacturer Address : 224-18, Hiraishi Ebisuno, Kawauchi-cho, Tokushima-shi, Tokushima, Japan
100
PharmaCompass offers a list of Procaterol API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Procaterol manufacturer or Procaterol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Procaterol manufacturer or Procaterol supplier.
A CI888 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CI888, including repackagers and relabelers. The FDA regulates CI888 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CI888 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 CI888 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A CI888 supplier is an individual or a company that provides CI888 active pharmaceutical ingredient (API) or CI888 finished formulations upon request. The CI888 suppliers may include CI888 API manufacturers, exporters, distributors and traders.
click here to find a list of CI888 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 CI888 Drug Master File in Korea (CI888 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of CI888. The MFDS reviews the CI888 KDMF as part of the drug registration process and uses the information provided in the CI888 KDMF to evaluate the safety and efficacy of the drug.
After submitting a CI888 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 CI888 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of CI888 suppliers with KDMF on PharmaCompass.
