01 1AbbVie Srl
02 1Laurus Labs Limited(Unit-4)
01 1AbbVie Korea Inc.
02 1Aging Life Science Co., Ltd.
01 2Lopinavir
01 1India
02 1Italy
Registrant Name : AbbVie Korea Inc.
Registration Date : 2008-06-27
Registration Number : 2578-2-ND
Manufacturer Name : AbbVie Srl
Manufacturer Address : SR 148 Pontina Km 52, Snc-Campoverde Di Aprilia-04011, Aprilia(LT), Italy
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2020-07-20
Registration Number : 434-19-ND
Manufacturer Name : Laurus Labs Limited(Unit-4)
Manufacturer Address : Plot No. 25, 25A to 25K, Lalamkoduru Village, Rambilli Mandal, Visakhapatnam - 531011...
A Lopinavir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lopinavir, including repackagers and relabelers. The FDA regulates Lopinavir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lopinavir 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 Lopinavir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lopinavir supplier is an individual or a company that provides Lopinavir active pharmaceutical ingredient (API) or Lopinavir finished formulations upon request. The Lopinavir suppliers may include Lopinavir API manufacturers, exporters, distributors and traders.
click here to find a list of Lopinavir 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 Lopinavir Drug Master File in Korea (Lopinavir KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Lopinavir. The MFDS reviews the Lopinavir KDMF as part of the drug registration process and uses the information provided in the Lopinavir KDMF to evaluate the safety and efficacy of the drug.
After submitting a Lopinavir 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 Lopinavir API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Lopinavir suppliers with KDMF on PharmaCompass.
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