01 1AKTINOS PHARMA PRIVATE LIMITED
02 1Arch Pharmalabs Limited
03 1Catalent Micron Technologies, Inc.
04 1Emcure Pharmaceuticals Limited
05 1LAURUS LABS LIMITED
06 1Mylan Laboratories Limited
07 2PROCOS S.p.A.
08 1Raks Pharma Pvt. Limited
09 1Siegfried Evionnaz SA
10 1Solara Active Pharma Sciences Limited
11 1Tianish Laboratories Private Limited
01 3FELBAMATE
02 1FELBAMATE MICRONIZED
03 7Felbamate
04 1felbamate
01 7India
02 2Italy
03 1Switzerland
04 2U.S.A
NDC Package Code : 22365-007
Start Marketing Date : 2009-01-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69988-0032
Start Marketing Date : 2004-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/1)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 14593-862
Start Marketing Date : 2023-12-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42385-721
Start Marketing Date : 2009-07-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46016-2541
Start Marketing Date : 2004-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46016-2542
Start Marketing Date : 2004-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47621-054
Start Marketing Date : 2017-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17381-554
Start Marketing Date : 2010-04-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 72643-037
Start Marketing Date : 2024-03-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-900
Start Marketing Date : 2024-03-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Felbamate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Felbamate, including repackagers and relabelers. The FDA regulates Felbamate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Felbamate 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 Felbamate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Felbamate supplier is an individual or a company that provides Felbamate active pharmaceutical ingredient (API) or Felbamate finished formulations upon request. The Felbamate suppliers may include Felbamate API manufacturers, exporters, distributors and traders.
click here to find a list of Felbamate 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 Felbamate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Felbamate 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 Felbamate 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 Felbamate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Felbamate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Felbamate suppliers with NDC on PharmaCompass.
We have 11 companies offering Felbamate
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
