"71921-221-06" National Drug Code (NDC)

Lacosamide 60 TABLET in 1 BOTTLE (71921-221-06)
(Florida Pharmaceutical Products, LLC)

NDC Code71921-221-06
Package Description60 TABLET in 1 BOTTLE (71921-221-06)
Product NDC71921-221
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLacosamide
Non-Proprietary NameLacosamide
Dosage FormTABLET
UsageORAL
Start Marketing Date20230921
Marketing Category NameANDA
Application NumberANDA208308
ManufacturerFlorida Pharmaceutical Products, LLC
Substance NameLACOSAMIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesDecreased Central Nervous System Disorganized Electrical Activity [PE]
DEA ScheduleCV

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