"50268-660-13" National Drug Code (NDC)

NDC Code	50268-660-13
Package Description	30 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-660-13) > 1 CAPSULE in 1 BLISTER PACK (50268-660-11)
Product NDC	50268-660
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Phenytoin Sodium
Proprietary Name Suffix	Extended
Non-Proprietary Name	Phenytoin Sodium
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20160607
Marketing Category Name	ANDA
Application Number	ANDA040765
Manufacturer	AvPAK
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]