NDC 31722-599

Rufinamide

Rufinamide

Rufinamide is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Camber Pharmaceuticals, Inc.. The primary component is Rufinamide.

Product ID31722-599_c3c611a2-394b-4427-e053-2a95a90a433f
NDC31722-599
Product TypeHuman Prescription Drug
Proprietary NameRufinamide
Generic NameRufinamide
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2021-05-11
Marketing CategoryANDA /
Application NumberANDA204993
Labeler NameCamber Pharmaceuticals, Inc.
Substance NameRUFINAMIDE
Active Ingredient Strength400 mg/1
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 31722-599-12

120 TABLET, FILM COATED in 1 BOTTLE (31722-599-12)
Marketing Start Date2021-05-11
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "Rufinamide" or generic name "Rufinamide"

NDCBrand NameGeneric Name
0054-0425RufinamideRufinamide
0054-0426RufinamideRufinamide
0054-0528RufinamideRufinamide
0378-2330Rufinamiderufinamide
0378-2331Rufinamiderufinamide
31722-598RufinamideRufinamide
31722-599RufinamideRufinamide
59651-563RUFINAMIDERUFINAMIDE
60687-643RufinamideRufinamide
67877-673RufinamideRufinamide
68180-797RufinamideRufinamide
68180-802RUFINAMIDErufinamide
68180-803RUFINAMIDErufinamide
69452-223RufinamideRufinamide
62856-582Banzelrufinamide
62856-583Banzelrufinamide
62856-584Banzelrufinamide

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.