01 1Zhejiang Lepu Pharmaceutical Co. , Ltd.
01 1Pazopanib Hydrochloride
01 1China
Registration Number : 307MF10025
Registrant's Address : No. 29 Binhai Road, Jiaojiang District, Taizhou City, Zhejiang Province, 318000, Chin...
Initial Date of Registration : 2025-02-07
Latest Date of Registration : 2025-02-07
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A CID10113978 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CID10113978, including repackagers and relabelers. The FDA regulates CID10113978 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CID10113978 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 CID10113978 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A CID10113978 supplier is an individual or a company that provides CID10113978 active pharmaceutical ingredient (API) or CID10113978 finished formulations upon request. The CID10113978 suppliers may include CID10113978 API manufacturers, exporters, distributors and traders.
click here to find a list of CID10113978 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The CID10113978 Drug Master File in Japan (CID10113978 JDMF) empowers CID10113978 API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the CID10113978 JDMF during the approval evaluation for pharmaceutical products. At the time of CID10113978 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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