01 1FIS Fabbrica Italiana Sintetici SpA@Catalent Micron Technologies Limited
02 1Formosa Laboratories, Inc.
03 1Glaxo Wellcome Manufacturing Pte. Ltd.@[Undifferentiated Manufacturer] Catalent Micron Technologies Limited
04 1Kekule Pharma Limited
05 1Thermo Fisher Scientific Cork Limited@Catalent Micron Technologies Limited
01 1Klasia Co., Ltd.
02 1M-Peak Korea Co., Ltd.
03 3Novartis Korea Ltd.
01 5Pazopanib hydrochloride
01 1India
02 1Italy
03 1Taiwan
04 1U.S.A
05 1United Kingdom
Registrant Name : Novartis Korea Ltd.
Registration Date : 2023-07-12
Registration Number : 196-26-ND
Manufacturer Name : FIS Fabbrica Italiana Sintet...
Manufacturer Address : Viale Milano, 26, 36075 Montecchio Maggiore (Vicenza), Italy@Crossways Boulevard, Cro...
Registrant Name : M-Peak Korea Co., Ltd.
Registration Date : 2020-10-21
Registration Number : Number 812-12-ND
Manufacturer Name : Formosa Laboratories, Inc.
Manufacturer Address : 36 Hoping Street, Louchu, Taoyuan 33842, Taiwan
Registrant Name : Novartis Korea Ltd.
Registration Date : 2012-07-31
Registration Number : 89-11-ND
Manufacturer Name : Glaxo Wellcome Manufacturing...
Manufacturer Address : 1 Pioneer Sector 1, Jurong, Singapore 628413@[Undifferentiated Manufacturer] Crossway...
Registrant Name : Klasia Co., Ltd.
Registration Date : 2021-10-25
Registration Number : No. 758-8-ND
Manufacturer Name : Kekule Pharma Limited
Manufacturer Address : MIA, Kazipally, Jinnaram Mandal, Sangareddy-502 319, Telangana State, India
Registrant Name : Novartis Korea Ltd.
Registration Date : 2021-03-23
Registration Number : 196-22-ND
Manufacturer Name : Thermo Fisher Scientific Cor...
Manufacturer Address : Currabinny, Carrigaline, County Cork, P43 AY66, Ireland@Crossways Boulevard, Crossway...
A Pazopanib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pazopanib, including repackagers and relabelers. The FDA regulates Pazopanib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pazopanib 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 Pazopanib manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pazopanib supplier is an individual or a company that provides Pazopanib active pharmaceutical ingredient (API) or Pazopanib finished formulations upon request. The Pazopanib suppliers may include Pazopanib API manufacturers, exporters, distributors and traders.
click here to find a list of Pazopanib 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 Pazopanib Drug Master File in Korea (Pazopanib KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Pazopanib. The MFDS reviews the Pazopanib KDMF as part of the drug registration process and uses the information provided in the Pazopanib KDMF to evaluate the safety and efficacy of the drug.
After submitting a Pazopanib 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 Pazopanib API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Pazopanib suppliers with KDMF on PharmaCompass.
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