01 1Olon SpA
02 1Sterling Biotech Limited
01 1Handok Co., Ltd.
02 1Korea United Pharmaceutical Co., Ltd.
01 2daunorubicin hydrochloride
01 1India
02 1Italy
Registrant Name : Handok Co., Ltd.
Registration Date : 2022-07-13
Registration Number : 20220713-210-J-1333
Manufacturer Name : Olon SpA
Manufacturer Address : Via Schiapparelli 2, 10036 Settimo Torinese (TO), Italy
Registrant Name : Korea United Pharmaceutical Co., Ltd.
Registration Date : 2021-04-09
Registration Number : 20210409-210-J-429
Manufacturer Name : Sterling Biotech Limited
Manufacturer Address : Jambusar State Highway, Village Masar-391 421, Ta.Padra, Vadodara, Gujarat, India
A Daunorubicin HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Daunorubicin HCl, including repackagers and relabelers. The FDA regulates Daunorubicin HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Daunorubicin HCl 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 Daunorubicin HCl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Daunorubicin HCl supplier is an individual or a company that provides Daunorubicin HCl active pharmaceutical ingredient (API) or Daunorubicin HCl finished formulations upon request. The Daunorubicin HCl suppliers may include Daunorubicin HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Daunorubicin HCl 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 Daunorubicin HCl Drug Master File in Korea (Daunorubicin HCl KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Daunorubicin HCl. The MFDS reviews the Daunorubicin HCl KDMF as part of the drug registration process and uses the information provided in the Daunorubicin HCl KDMF to evaluate the safety and efficacy of the drug.
After submitting a Daunorubicin HCl 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 Daunorubicin HCl API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Daunorubicin HCl suppliers with KDMF on PharmaCompass.
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