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 Pramoxine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pramoxine Hydrochloride, including repackagers and relabelers. The FDA regulates Pramoxine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pramoxine 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 Pramoxine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Pramoxine Hydrochloride supplier is an individual or a company that provides Pramoxine Hydrochloride active pharmaceutical ingredient (API) or Pramoxine Hydrochloride finished formulations upon request. The Pramoxine Hydrochloride suppliers may include Pramoxine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Pramoxine 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 Pramoxine Hydrochloride Drug Master File in Korea (Pramoxine Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Pramoxine Hydrochloride. The MFDS reviews the Pramoxine Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Pramoxine Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Pramoxine 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 Pramoxine Hydrochloride API can apply through the Korea Drug Master File (KDMF).
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