"0173-0754-00" National Drug Code (NDC)

Lamictal 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0173-0754-00)
(GlaxoSmithKline LLC)

NDC Code0173-0754-00
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0173-0754-00)
Product NDC0173-0754
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLamictal
Proprietary Name SuffixXr
Non-Proprietary NameLamotrigine
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20090706
Marketing Category NameNDA
Application NumberNDA022115
ManufacturerGlaxoSmithKline LLC
Substance NameLAMOTRIGINE
Strength25
Strength Unitmg/1
Pharmacy ClassesAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Dihydrofolate Reductase Inhibitors [MoA], Mood Stabilizer [EPC], Organic Cation Transporter 2 Inhibitors [MoA]

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