01 1Amino Chemicals Ltd
02 2Dipharma Francis S.r.l.
03 1Glenmark Life Sciences Limited
04 1Hetero Drugs Limited
05 1MSN Laboratories Private Limited
06 1MSN Life Sciences Private Limited
07 1n.v. Ajinomoto OmniChem S.A.
01 7Rufinamide
02 1rufinamide
01 4India
02 2Italy
03 1Japan
04 1Malta
NDC Package Code : 50923-0614
Start Marketing Date : 2004-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66039-881
Start Marketing Date : 2012-10-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66005-0037
Start Marketing Date : 2011-01-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0662
Start Marketing Date : 2021-04-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0661
Start Marketing Date : 2021-04-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65977-0068
Start Marketing Date : 2008-11-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69766-050
Start Marketing Date : 2018-04-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14501-0058
Start Marketing Date : 2010-03-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Rufinamide 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 Rufinamide manufacturer or Rufinamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rufinamide manufacturer or Rufinamide supplier.
PharmaCompass also assists you with knowing the Rufinamide API Price utilized in the formulation of products. Rufinamide API Price is not always fixed or binding as the Rufinamide Price is obtained through a variety of data sources. The Rufinamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Banzel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Banzel, including repackagers and relabelers. The FDA regulates Banzel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Banzel 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 Banzel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Banzel supplier is an individual or a company that provides Banzel active pharmaceutical ingredient (API) or Banzel finished formulations upon request. The Banzel suppliers may include Banzel API manufacturers, exporters, distributors and traders.
click here to find a list of Banzel 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 Banzel as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Banzel 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 Banzel 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 Banzel and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Banzel NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Banzel suppliers with NDC on PharmaCompass.
We have 6 companies offering Banzel
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