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, Luncheng 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, Luncheng 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
A Oxytetracycline Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxytetracycline Hydrochloride, including repackagers and relabelers. The FDA regulates Oxytetracycline Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxytetracycline 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 Oxytetracycline Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxytetracycline Hydrochloride supplier is an individual or a company that provides Oxytetracycline Hydrochloride active pharmaceutical ingredient (API) or Oxytetracycline Hydrochloride finished formulations upon request. The Oxytetracycline Hydrochloride suppliers may include Oxytetracycline Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Oxytetracycline Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Oxytetracycline Hydrochloride Drug Master File in Japan (Oxytetracycline Hydrochloride JDMF) empowers Oxytetracycline Hydrochloride 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 Oxytetracycline Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Oxytetracycline Hydrochloride 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 Oxytetracycline Hydrochloride suppliers with JDMF on PharmaCompass.
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