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"51672-4131-3" National Drug Code (NDC)

Lamotrigine 1000 TABLET in 1 BOTTLE (51672-4131-3)
(Taro Pharmaceuticals U.S.A., Inc.)

NDC Code51672-4131-3
Package Description1000 TABLET in 1 BOTTLE (51672-4131-3)
Product NDC51672-4131
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLamotrigine
Non-Proprietary NameLamotrigine
Dosage FormTABLET
UsageORAL
Start Marketing Date20090127
Marketing Category NameANDA
Application NumberANDA078525
ManufacturerTaro Pharmaceuticals U.S.A., Inc.
Substance NameLAMOTRIGINE
Strength100
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/51672-4131-3





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