Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
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Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Registrant Name : Bansen Co., Ltd.
Registration Date : 2016-01-08
Registration Number : 20160108-171-I-474-06
Manufacturer Name : Zhejiang Hengkang Pharmaceut...
Manufacturer Address : No.1 Longxiang Road, Hairun Street, Sanmen, Zhejiang, China
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2020-11-13
Registration Number : 20160108-171-I-474-06(1)
Manufacturer Name : Zhejiang Hengkang Pharmaceut...
Manufacturer Address : No.1 Longxiang Road, Hairun Street, Sanmen, Zhejiang, China
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PharmaCompass offers a list of Pranlukast API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Pranlukast manufacturer or Pranlukast supplier for your needs.
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A Pranlukast manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pranlukast, including repackagers and relabelers. The FDA regulates Pranlukast manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pranlukast 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 Pranlukast supplier is an individual or a company that provides Pranlukast active pharmaceutical ingredient (API) or Pranlukast finished formulations upon request. The Pranlukast suppliers may include Pranlukast 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 Pranlukast Drug Master File in Korea (Pranlukast KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Pranlukast. The MFDS reviews the Pranlukast KDMF as part of the drug registration process and uses the information provided in the Pranlukast KDMF to evaluate the safety and efficacy of the drug.
After submitting a Pranlukast 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 Pranlukast API can apply through the Korea Drug Master File (KDMF).
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