"50090-0029-2" National Drug Code (NDC)

NDC Code	50090-0029-2
Package Description	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-0029-2)
Product NDC	50090-0029
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Dilantin
Non-Proprietary Name	Phenytoin Sodium
Dosage Form	CAPSULE, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	19760827
Marketing Category Name	ANDA
Application Number	ANDA084349
Manufacturer	A-S Medication Solutions
Substance Name	PHENYTOIN SODIUM
Strength	100
Strength Unit	mg/1
Pharmacy Classes	Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Cytochrome P450 1A2 Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA],Cytochrome P450 2C8 Inducers [MoA],Cytochrome P450 2C19 Inducers [MoA],Cytochrome P450 2D6 Inducers [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2C9 Inducers [MoA]