"51991-351-05" National Drug Code (NDC)

Lacosamide 500 TABLET, FILM COATED in 1 BOTTLE (51991-351-05)
(Breckenridge Pharmaceutical, Inc.)

NDC Code51991-351-05
Package Description500 TABLET, FILM COATED in 1 BOTTLE (51991-351-05)
Product NDC51991-351
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLacosamide
Non-Proprietary NameLacosamide
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220318
Marketing Category NameANDA
Application NumberANDA204921
ManufacturerBreckenridge Pharmaceutical, Inc.
Substance NameLACOSAMIDE
Strength200
Strength Unitmg/1
Pharmacy ClassesDecreased Central Nervous System Disorganized Electrical Activity [PE]
DEA ScheduleCV

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