"50090-2903-0" National Drug Code (NDC)

NDC Code	50090-2903-0
Package Description	32 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-2903-0) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC	50090-2903
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Phenytoin Sodium
Non-Proprietary Name	Phenytoin Sodium
Dosage Form	CAPSULE, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20061212
Marketing Category Name	ANDA
Application Number	ANDA040621
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]