"0904-7199-07" National Drug Code (NDC)

NDC Code	0904-7199-07
Package Description	30 BLISTER PACK in 1 CARTON (0904-7199-07) / 1 TABLET, CHEWABLE in 1 BLISTER PACK
Product NDC	0904-7199
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Phenytoin
Non-Proprietary Name	Phenytoin
Dosage Form	TABLET, CHEWABLE
Usage	ORAL
Start Marketing Date	20140417
Marketing Category Name	ANDA
Application Number	ANDA200565
Manufacturer	Major Pharmaceuticals
Substance Name	PHENYTOIN
Strength	50
Strength Unit	mg/1
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]