01 1Syn-Tech Chem &Pharm. Co., Ltd.
01 1Wooshin Labotach Co., Ltd.
01 1Pramoxine hydrochloride
01 1Taiwan
Registrant Name : Wooshin Labotach Co., Ltd.
Registration Date : 2022-10-20
Registration Number : 20221020-211-J-1385
Manufacturer Name : Syn-Tech Chem &Pharm. Co., L...
Manufacturer Address : No. 168 Kai Yuan Rd., Hsin-Ying, Tainan City, 73055, Taiwan
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PharmaCompass offers a list of Pramoxine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Pramoxine Hydrochloride manufacturer or Pramoxine Hydrochloride supplier for your needs.
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A Pramocaine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pramocaine Hydrochloride, including repackagers and relabelers. The FDA regulates Pramocaine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pramocaine 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.
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A Pramocaine Hydrochloride supplier is an individual or a company that provides Pramocaine Hydrochloride active pharmaceutical ingredient (API) or Pramocaine Hydrochloride finished formulations upon request. The Pramocaine Hydrochloride suppliers may include Pramocaine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Pramocaine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Pramocaine Hydrochloride Drug Master File in Korea (Pramocaine Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Pramocaine Hydrochloride. The MFDS reviews the Pramocaine Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Pramocaine Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Pramocaine 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 Pramocaine Hydrochloride API can apply through the Korea Drug Master File (KDMF).
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