"60505-0183-5" National Drug Code (NDC)

NDC Code	60505-0183-5
Package Description	500 TABLET in 1 BOTTLE (60505-0183-5)
Product NDC	60505-0183
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carbamazepine
Non-Proprietary Name	Carbamazepine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20020901
End Marketing Date	20230121
Marketing Category Name	ANDA
Application Number	ANDA075948
Manufacturer	Apotex Corp.
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]