01 1Qidong Dongyue Pharmaceutical Co., Ltd
01 1Kukjeon Pharmaceutical Co., Ltd.
01 1Diphenhydramine hydrochloride
01 1China
Registrant Name : Kukjeon Pharmaceutical Co., Ltd.
Registration Date : 2017-09-07
Registration Number : 20170907-211-J-3
Manufacturer Name : Qidong Dongyue Pharmaceutica...
Manufacturer Address : No.268 Shanghai Rd., Binjiang Fine Chemical Industry Zone, Qidong City, China
A Diphenhydramine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diphenhydramine Hydrochloride, including repackagers and relabelers. The FDA regulates Diphenhydramine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diphenhydramine Hydrochloride 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 Diphenhydramine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diphenhydramine Hydrochloride supplier is an individual or a company that provides Diphenhydramine Hydrochloride active pharmaceutical ingredient (API) or Diphenhydramine Hydrochloride finished formulations upon request. The Diphenhydramine Hydrochloride suppliers may include Diphenhydramine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Diphenhydramine Hydrochloride 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 Diphenhydramine Hydrochloride Drug Master File in Korea (Diphenhydramine Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Diphenhydramine Hydrochloride. The MFDS reviews the Diphenhydramine Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Diphenhydramine Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Diphenhydramine Hydrochloride 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 Diphenhydramine Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Diphenhydramine Hydrochloride suppliers with KDMF on PharmaCompass.
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