01 2Syn-Tech Chem & Pharm. Co., Ltd.
01 1Hwail Pharmaceutical Co., Ltd.
02 1Wooshin Labotech Co., Ltd.
01 2chlorpheniramine hydrochloride
01 2Taiwan
chlorpheniramine hydrochloride
Registrant Name : Wooshin Labotech Co., Ltd.
Registration Date : 2021-07-15
Registration Number : 20210715-209-J-979
Manufacturer Name : Syn-Tech Chem & Pharm. Co., ...
Manufacturer Address : No. 168 Kai Yuan Rd., Hsin-Ying, Tainan City, 73055, Taiwan
chlorpheniramine hydrochloride
Registrant Name : Hwail Pharmaceutical Co., Ltd.
Registration Date : 2021-12-02
Registration Number : 20210715-209-J-979(1)
Manufacturer Name : Syn-Tech Chem & Pharm. Co., ...
Manufacturer Address : No. 168, Kai Yuan Rd., Hsin-Ying, Tainan City, 73055, Taiwan
A Cloperastine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cloperastine, including repackagers and relabelers. The FDA regulates Cloperastine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cloperastine 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 Cloperastine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cloperastine supplier is an individual or a company that provides Cloperastine active pharmaceutical ingredient (API) or Cloperastine finished formulations upon request. The Cloperastine suppliers may include Cloperastine API manufacturers, exporters, distributors and traders.
click here to find a list of Cloperastine 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 Cloperastine Drug Master File in Korea (Cloperastine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Cloperastine. The MFDS reviews the Cloperastine KDMF as part of the drug registration process and uses the information provided in the Cloperastine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Cloperastine 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 Cloperastine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Cloperastine suppliers with KDMF on PharmaCompass.
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