"49999-616-90" National Drug Code (NDC)

NDC Code	49999-616-90
Package Description	90 TABLET in 1 BOTTLE (49999-616-90)
Product NDC	49999-616
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carbamazepine
Non-Proprietary Name	Carbamazepine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20091023
Marketing Category Name	ANDA
Application Number	ANDA077272
Manufacturer	Lake Erie Medical DBA Quality Care Products LLC
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]