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...
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A CAS-155213-67-5 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-155213-67-5, including repackagers and relabelers. The FDA regulates CAS-155213-67-5 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-155213-67-5 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A CAS-155213-67-5 supplier is an individual or a company that provides CAS-155213-67-5 active pharmaceutical ingredient (API) or CAS-155213-67-5 finished formulations upon request. The CAS-155213-67-5 suppliers may include CAS-155213-67-5 API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a CAS-155213-67-5 Drug Master File in Korea (CAS-155213-67-5 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of CAS-155213-67-5. The MFDS reviews the CAS-155213-67-5 KDMF as part of the drug registration process and uses the information provided in the CAS-155213-67-5 KDMF to evaluate the safety and efficacy of the drug.
After submitting a CAS-155213-67-5 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 CAS-155213-67-5 API can apply through the Korea Drug Master File (KDMF).
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We have 3 companies offering CAS-155213-67-5
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