"51672-4069-2" National Drug Code (NDC)

NDC Code	51672-4069-2
Package Description	1 BOTTLE in 1 CARTON (51672-4069-2) / 237 mL in 1 BOTTLE
Product NDC	51672-4069
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	Sun Pharmaceutical Industries, Inc.
Substance Name	PHENYTOIN
Strength	125
Strength Unit	mg/5mL
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]