"58151-110-88" National Drug Code (NDC)

NDC Code	58151-110-88
Package Description	100 BLISTER PACK in 1 CARTON (58151-110-88) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (58151-110-32)
Product NDC	58151-110
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Dilantin
Non-Proprietary Name	Extended Phenytoin Sodium
Dosage Form	CAPSULE, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20241206
Marketing Category Name	ANDA
Application Number	ANDA084349
Manufacturer	Viatris Specialty LLC
Substance Name	PHENYTOIN SODIUM
Strength	100
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]