"0904-7079-57" National Drug Code (NDC)

NDC Code	0904-7079-57
Package Description	50 CUP, UNIT-DOSE in 1 CASE (0904-7079-57) > 4 mL in 1 CUP, UNIT-DOSE (0904-7079-24)
Product NDC	0904-7079
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Phenytoin
Non-Proprietary Name	Phenytoin
Dosage Form	SUSPENSION
Usage	ORAL
Start Marketing Date	20040408
Marketing Category Name	ANDA
Application Number	ANDA040521
Manufacturer	Major Pharmaceuticals
Substance Name	PHENYTOIN
Strength	100
Strength Unit	mg/4mL
Pharmacy Classes	Anti-epileptic Agent [EPC], Cytochrome P450 1A2 Inducers [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inducers [MoA], Cytochrome P450 2C8 Inducers [MoA], Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 2D6 Inducers [MoA], Cytochrome P450 3A Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE]