01 1AbbVie Srl
02 1Hetero Drugs Limited
03 1Laurus Labs Limited(Unit-3)
01 1AbbVie Korea Inc.
02 1Aging Life Science Co., Ltd.
03 1Korea Pfizer Pharmaceutical Co., Ltd.
01 3Ritonavir
01 2India
02 1Italy
Registrant Name : AbbVie Korea Inc.
Registration Date : 2008-06-27
Registration Number : 2578-1-ND
Manufacturer Name : AbbVie Srl
Manufacturer Address : SR 148 Pontina Km 52, Snc-Campoverde Di Aprilia-04011, Aprilia(LT), Italy
Registrant Name : Korea Pfizer Pharmaceutical Co., Ltd.
Registration Date : 2023-07-14
Registration Number : Number 87-36-ND
Manufacturer Name : Hetero Drugs Limited
Manufacturer Address : Unit-IX, Plot No.1, Hetero Infrastructure Ltd.- SEZ, N. Narasapuram Village, Nakkapal...
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2020-07-07
Registration Number : Su434-13-ND
Manufacturer Name : Laurus Labs Limited(Unit-3)
Manufacturer Address : Plot No. 18, Jawaharlal Nehru Pharma City, Parawada, Anakapalli 531021, Andhra Prades...
A Ritonavir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ritonavir, including repackagers and relabelers. The FDA regulates Ritonavir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ritonavir 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 Ritonavir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ritonavir supplier is an individual or a company that provides Ritonavir active pharmaceutical ingredient (API) or Ritonavir finished formulations upon request. The Ritonavir suppliers may include Ritonavir API manufacturers, exporters, distributors and traders.
click here to find a list of Ritonavir 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 Ritonavir Drug Master File in Korea (Ritonavir KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Ritonavir. The MFDS reviews the Ritonavir KDMF as part of the drug registration process and uses the information provided in the Ritonavir KDMF to evaluate the safety and efficacy of the drug.
After submitting a Ritonavir 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 Ritonavir API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Ritonavir suppliers with KDMF on PharmaCompass.
We have 3 companies offering Ritonavir
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