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