"60687-335-21" National Drug Code (NDC)

NDC Code	60687-335-21
Package Description	30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-335-21) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-335-11)
Product NDC	60687-335
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carbamazepine
Non-Proprietary Name	Carbamazepine
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20190801
Marketing Category Name	ANDA
Application Number	ANDA078115
Manufacturer	American Health Packaging
Substance Name	CARBAMAZEPINE
Strength	400
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]