01 1Yancheng Suhai Pharmaceutical Co., Ltd
02 1Yancheng Suhai Pharmaceutical Co.,Ltd
01 2Sam-O Pharmaceutical Co., Ltd.
01 2Doxycycline Hyclate
01 2China
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2022-05-27
Registration Number : 20220527-101-F-98-05
Manufacturer Name : Yancheng Suhai Pharmaceutica...
Manufacturer Address : Huafeng Industrial Park, Dafeng Port Economic Development Zone, Dafeng District, Yanc...
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2011-06-30
Registration Number : 20110630-101-F-59-02
Manufacturer Name : Yancheng Suhai Pharmaceutica...
Manufacturer Address : No. 92 E.Jiankang Road, Dafeng City, Jiangsu, China
95
PharmaCompass offers a list of Doxycycline Hyclate 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 Doxycycline Hyclate manufacturer or Doxycycline Hyclate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Doxycycline Hyclate manufacturer or Doxycycline Hyclate supplier.
A DOXY 200 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DOXY 200, including repackagers and relabelers. The FDA regulates DOXY 200 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DOXY 200 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 DOXY 200 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A DOXY 200 supplier is an individual or a company that provides DOXY 200 active pharmaceutical ingredient (API) or DOXY 200 finished formulations upon request. The DOXY 200 suppliers may include DOXY 200 API manufacturers, exporters, distributors and traders.
click here to find a list of DOXY 200 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 DOXY 200 Drug Master File in Korea (DOXY 200 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of DOXY 200. The MFDS reviews the DOXY 200 KDMF as part of the drug registration process and uses the information provided in the DOXY 200 KDMF to evaluate the safety and efficacy of the drug.
After submitting a DOXY 200 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 DOXY 200 API can apply through the Korea Drug Master File (KDMF).
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