"68788-9492-1" National Drug Code (NDC)

NDC Code	68788-9492-1
Package Description	100 TABLET in 1 BOTTLE (68788-9492-1)
Product NDC	68788-9492
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carbamazepine
Non-Proprietary Name	Carbamazepine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20140402
Marketing Category Name	ANDA
Application Number	ANDA077272
Manufacturer	Preferred Pharmaceuticals, 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]