"68382-556-30" National Drug Code (NDC)

NDC Code	68382-556-30
Package Description	10 BLISTER PACK in 1 CARTON (68382-556-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC	68382-556
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Carbamazepine
Non-Proprietary Name	Carbamazepine
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20190312
Marketing Category Name	ANDA
Application Number	ANDA205571
Manufacturer	Zydus Pharmaceuticals (USA) Inc.
Substance Name	CARBAMAZEPINE
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Cytochrome P450 1A2 Inducers [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inducers [MoA], Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 3A4 Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]