"62332-731-10" National Drug Code (NDC)

NDC Code	62332-731-10
Package Description	100 BLISTER PACK in 1 CARTON (62332-731-10) / 10 TABLET in 1 BLISTER PACK
Product NDC	62332-731
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carbamazepine
Non-Proprietary Name	Carbamazepine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20241231
Marketing Category Name	ANDA
Application Number	ANDA216623
Manufacturer	Alembic 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]