01 1Chifeng Pharmaceutical Co. , Ltd.
02 2Hebei Shengxue Dacheng Pharmaceutical Co. , Ltd.
01 3Oxytetracycline hydrochloride
01 2China
02 1South Korea
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 : 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 : 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, Price,and more, enabling you to easily find the right Oxytetracycline Hydrochloride manufacturer or Oxytetracycline Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxytetracycline Hydrochloride manufacturer or Oxytetracycline Hydrochloride supplier.
PharmaCompass also assists you with knowing the Oxytetracycline Hydrochloride API Price utilized in the formulation of products. Oxytetracycline Hydrochloride API Price is not always fixed or binding as the Oxytetracycline Hydrochloride Price is obtained through a variety of data sources. The Oxytetracycline Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxyvet manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxyvet, including repackagers and relabelers. The FDA regulates Oxyvet manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxyvet 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 Oxyvet manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxyvet supplier is an individual or a company that provides Oxyvet active pharmaceutical ingredient (API) or Oxyvet finished formulations upon request. The Oxyvet suppliers may include Oxyvet API manufacturers, exporters, distributors and traders.
click here to find a list of Oxyvet 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 Oxyvet Drug Master File in Japan (Oxyvet JDMF) empowers Oxyvet 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 Oxyvet JDMF during the approval evaluation for pharmaceutical products. At the time of Oxyvet 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 Oxyvet suppliers with JDMF on PharmaCompass.
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