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 : 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
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
A Pranlukast Hydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pranlukast Hydrate, including repackagers and relabelers. The FDA regulates Pranlukast Hydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pranlukast Hydrate 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 Hydrate supplier is an individual or a company that provides Pranlukast Hydrate active pharmaceutical ingredient (API) or Pranlukast Hydrate finished formulations upon request. The Pranlukast Hydrate suppliers may include Pranlukast Hydrate 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 Hydrate Drug Master File in Korea (Pranlukast Hydrate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Pranlukast Hydrate. The MFDS reviews the Pranlukast Hydrate KDMF as part of the drug registration process and uses the information provided in the Pranlukast Hydrate KDMF to evaluate the safety and efficacy of the drug.
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