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
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PharmaCompass offers a list of Oxethazaine 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 Oxethazaine manufacturer or Oxethazaine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxethazaine manufacturer or Oxethazaine supplier.
PharmaCompass also assists you with knowing the Oxethazaine API Price utilized in the formulation of products. Oxethazaine API Price is not always fixed or binding as the Oxethazaine Price is obtained through a variety of data sources. The Oxethazaine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
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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