01 1Aarti Pharmalabs limited(Unit-IV)
02 1Zhejiang Huahai Pharmaceutical Co., Ltd. Ltd
01 1Aging Life Science Co., Ltd.
02 1Menarini Korea Co., Ltd.
01 2Ranolazine
01 1China
02 1Blank
Registrant Name : Menarini Korea Co., Ltd.
Registration Date : 2020-03-13
Registration Number : 11-2-ND
Manufacturer Name : Zhejiang Huahai Pharmaceutic...
Manufacturer Address : Chuannan, Duqiao, Linhai, Zhejiang, 317016, China
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2024-10-07
Registration Number : 434-66-ND
Manufacturer Name : Aarti Pharmalabs limited(Uni...
Manufacturer Address : Plot No: E–50, 50/1 & 59/1, MIDC, Tarapur, Taluka & District: Palghar, 401 506, Mah...
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A Ranolazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ranolazine, including repackagers and relabelers. The FDA regulates Ranolazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ranolazine 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 Ranolazine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ranolazine supplier is an individual or a company that provides Ranolazine active pharmaceutical ingredient (API) or Ranolazine finished formulations upon request. The Ranolazine suppliers may include Ranolazine API manufacturers, exporters, distributors and traders.
click here to find a list of Ranolazine 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 Ranolazine Drug Master File in Korea (Ranolazine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ranolazine. The MFDS reviews the Ranolazine KDMF as part of the drug registration process and uses the information provided in the Ranolazine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ranolazine 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 Ranolazine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Ranolazine suppliers with KDMF on PharmaCompass.
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