"70518-2242-0" National Drug Code (NDC)

NDC Code	70518-2242-0
Package Description	180 TABLET in 1 BOTTLE, PLASTIC (70518-2242-0)
Product NDC	70518-2242
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carbamazepine
Non-Proprietary Name	Carbamazepine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20190731
Marketing Category Name	ANDA
Application Number	ANDA074649
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]