01 1Syn-Tech Chem. & Pharm. Co. , Ltd.
01 1Oxethazaine "production-only"
01 1Taiwan
Oxethazaine "For manufacturing purposes only"
Registration Number : 223MF10076
Registrant's Address : No. 168 Kai-Yuan Rd. , Hsin-Ying Tainan City, 73055. Taiwan
Initial Date of Registration : 2011-06-07
Latest Date of Registration : 2017-09-28
A Oxethazaine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxethazaine, including repackagers and relabelers. The FDA regulates Oxethazaine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxethazaine 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 Oxethazaine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxethazaine supplier is an individual or a company that provides Oxethazaine active pharmaceutical ingredient (API) or Oxethazaine finished formulations upon request. The Oxethazaine suppliers may include Oxethazaine API manufacturers, exporters, distributors and traders.
click here to find a list of Oxethazaine 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 Oxethazaine Drug Master File in Japan (Oxethazaine JDMF) empowers Oxethazaine 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 Oxethazaine JDMF during the approval evaluation for pharmaceutical products. At the time of Oxethazaine 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 Oxethazaine suppliers with JDMF on PharmaCompass.
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