"70518-0902-0" National Drug Code (NDC)

NDC Code	70518-0902-0
Package Description	30 TABLET in 1 BLISTER PACK (70518-0902-0)
Product NDC	70518-0902
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carbamazepine
Non-Proprietary Name	Carbamazepine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20171212
Marketing Category Name	ANDA
Application Number	ANDA077272
Manufacturer	REMEDYREPACK 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]