01 1Fagron Services B.V.
02 1Siegfried Evionnaz SA
01 1Benoxinate Hydrochloride
02 1Oxybuprocaine Hydrochloride
01 1Netherlands
02 1Switzerland
NDC Package Code : 76003-0842
Start Marketing Date : 2018-02-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 17381-253
Start Marketing Date : 2010-05-11
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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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 Benoxinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benoxinate, including repackagers and relabelers. The FDA regulates Benoxinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benoxinate 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 Benoxinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Benoxinate supplier is an individual or a company that provides Benoxinate active pharmaceutical ingredient (API) or Benoxinate finished formulations upon request. The Benoxinate suppliers may include Benoxinate API manufacturers, exporters, distributors and traders.
click here to find a list of Benoxinate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Benoxinate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Benoxinate API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Benoxinate as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Benoxinate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Benoxinate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Benoxinate suppliers with NDC on PharmaCompass.
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