NDC 60687-643

Rufinamide

Rufinamide

Rufinamide is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by American Health Packaging. The primary component is Rufinamide.

Product ID60687-643_e0c90c5c-48fe-5369-e053-2a95a90a9d0e
NDC60687-643
Product TypeHuman Prescription Drug
Proprietary NameRufinamide
Generic NameRufinamide
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2022-06-20
Marketing CategoryANDA /
Application NumberANDA205075
Labeler NameAmerican Health Packaging
Substance NameRUFINAMIDE
Active Ingredient Strength400 mg/1
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 60687-643-21

30 BLISTER PACK in 1 CARTON (60687-643-21) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-643-11)
Marketing Start Date2022-06-20
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
60687-643RufinamideRufinamide
67877-673RufinamideRufinamide
68462-713rufinamiderufinamide
68462-714rufinamiderufinamide
69452-223RufinamideRufinamide
62856-582Banzelrufinamide
62856-583Banzelrufinamide
62856-584Banzelrufinamide

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