"49349-677-24" National Drug Code (NDC)

NDC Code	49349-677-24
Package Description	200 TABLET in 1 BLISTER PACK (49349-677-24)
Product NDC	49349-677
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carbamazepine
Non-Proprietary Name	Carbamazepine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20110516
End Marketing Date	20171128
Marketing Category Name	ANDA
Application Number	ANDA070541
Manufacturer	REMEDYREPACK INC.
Substance Name	CARBAMAZEPINE
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC],Cytochrome P450 3A4 Inducers [MoA],Cytochrome P450 1A2 Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA],Cytochrome P450 2C9 Inducers [MoA],Cytochrome P450 2C19 Inducers [MoA]