01 1Chifeng Pharmaceutical Co. , Ltd.
02 2Hebei Shengxue Dacheng Pharmaceutical Co. , Ltd.
01 3Oxytetracycline hydrochloride
01 2China
02 1South Korea
Registration Number : 228MF10098
Registrant's Address : No. 50 Shengxue Road, Luancheng Shijiazhuang, Hebei Province, China
Initial Date of Registration : 2016-05-23
Latest Date of Registration : 2016-05-23
Registration Number : 222MF10078
Registrant's Address : No. 50 Shengxue Road, Luancheng Shijiazhuang, Hebei Province, China
Initial Date of Registration : 2010-03-09
Latest Date of Registration : 2014-02-28
Registration Number : 221MF10020
Registrant's Address : 84 Yidong Street, Hongshan District, Chifeng 024001, Inner Mongolia, China
Initial Date of Registration : 2009-01-28
Latest Date of Registration : 2009-01-28
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PharmaCompass offers a list of Oxytetracycline 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 Oxytetracycline Hydrochloride manufacturer or Oxytetracycline Hydrochloride supplier for your needs.
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A Oxy-Rivo manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxy-Rivo, including repackagers and relabelers. The FDA regulates Oxy-Rivo manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxy-Rivo 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 Oxy-Rivo manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Oxy-Rivo supplier is an individual or a company that provides Oxy-Rivo active pharmaceutical ingredient (API) or Oxy-Rivo finished formulations upon request. The Oxy-Rivo suppliers may include Oxy-Rivo API manufacturers, exporters, distributors and traders.
click here to find a list of Oxy-Rivo suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Oxy-Rivo Drug Master File in Japan (Oxy-Rivo JDMF) empowers Oxy-Rivo API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Oxy-Rivo JDMF during the approval evaluation for pharmaceutical products. At the time of Oxy-Rivo JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Oxy-Rivo suppliers with JDMF on PharmaCompass.
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