"51672-4005-3" National Drug Code (NDC)

NDC Code	51672-4005-3
Package Description	1000 TABLET in 1 BOTTLE (51672-4005-3)
Product NDC	51672-4005
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carbamazepine
Non-Proprietary Name	Carbamazepine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19961003
Marketing Category Name	ANDA
Application Number	ANDA074649
Manufacturer	Taro Pharmaceuticals U.S.A., Inc.
Substance Name	CARBAMAZEPINE
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Cytochrome P450 1A2 Inducers [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inducers [MoA], Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 3A4 Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]