"0615-3505-39" National Drug Code (NDC)

NDC Code	0615-3505-39
Package Description	30 TABLET in 1 BLISTER PACK (0615-3505-39)
Product NDC	0615-3505
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carbamazepine
Non-Proprietary Name	Carbamazepine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19900930
End Marketing Date	20240430
Marketing Category Name	ANDA
Application Number	ANDA070541
Manufacturer	NCS HealthCare of KY, LLC dba Vangard Labs
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]