"68462-713-30" National Drug Code (NDC)

Rufinamide 30 TABLET, FILM COATED in 1 BOTTLE (68462-713-30)
(Glenmark Pharmaceuticals Inc., USA)

NDC Code68462-713-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68462-713-30)
Product NDC68462-713
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRufinamide
Non-Proprietary NameRufinamide
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160516
Marketing Category NameANDA
Application NumberANDA205075
ManufacturerGlenmark Pharmaceuticals Inc., USA
Substance NameRUFINAMIDE
Strength200
Strength Unitmg/1

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