01 1Hanmi Fine Chemical Co., Ltd.
02 1JW Pharmaceutical Co., Ltd.
03 1JW Pharmaceutical Co., Ltd. @[Manufacturer of Method 2 Starting Material (Itraconazole)] Nosch Lab. PVT. LTD @[Manufacturer of Method 3 Starting Material (Itraconazole)] Nosch Lab. PVT. LTD Unit-II @[Manufacturer of Method 2 Starting Material (Itraconazol
04 2Janssen Pharmaceutica NV
05 1Janssen Pharmaceutical Sciences Unlimited Company
06 1M/s. RADISON LABS PRIVATE LIMITED
07 1NOSCH LABS PRIVATE LIMITED@Nosch Labs Pvt. Ltd (Unit IV)
08 1Nosch Lab. PVT.LTD@Nosch Labs Pvt. Ltd (Unit IV)
09 3Nosch Labs Pvt. Ltd (Unit-II)
10 6SMS Pharmaceuticals Limited
11 2Vasudha Pharma Chem Limited (Unit-III)
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A MolPort-000-883-864 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-000-883-864, including repackagers and relabelers. The FDA regulates MolPort-000-883-864 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-000-883-864 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 MolPort-000-883-864 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A MolPort-000-883-864 supplier is an individual or a company that provides MolPort-000-883-864 active pharmaceutical ingredient (API) or MolPort-000-883-864 finished formulations upon request. The MolPort-000-883-864 suppliers may include MolPort-000-883-864 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-000-883-864 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 MolPort-000-883-864 Drug Master File in Korea (MolPort-000-883-864 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of MolPort-000-883-864. The MFDS reviews the MolPort-000-883-864 KDMF as part of the drug registration process and uses the information provided in the MolPort-000-883-864 KDMF to evaluate the safety and efficacy of the drug.
After submitting a MolPort-000-883-864 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 MolPort-000-883-864 API can apply through the Korea Drug Master File (KDMF).
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