"68071-4313-1" National Drug Code (NDC)

NDC Code	68071-4313-1
Package Description	120 TABLET in 1 BOTTLE (68071-4313-1)
Product NDC	68071-4313
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carbamazepine
Non-Proprietary Name	Carbamazepine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20020901
Marketing Category Name	ANDA
Application Number	ANDA075948
Manufacturer	NuCare Pharmaceuticals,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]