"50742-257-01" National Drug Code (NDC)

NDC Code	50742-257-01
Package Description	100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50742-257-01)
Product NDC	50742-257
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carbamazepine
Non-Proprietary Name	Carbamazepine
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20230801
Marketing Category Name	ANDA
Application Number	ANDA216404
Manufacturer	Ingenus Pharmaceuticals, LLC
Substance Name	CARBAMAZEPINE
Strength	100
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]