"70518-2554-0" National Drug Code (NDC)

NDC Code	70518-2554-0
Package Description	10 CUP in 1 BOX (70518-2554-0) > 10 mL in 1 CUP (70518-2554-1)
Product NDC	70518-2554
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Phenytoin
Non-Proprietary Name	Phenytoin
Dosage Form	SUSPENSION
Usage	ORAL
Start Marketing Date	20200123
Marketing Category Name	ANDA
Application Number	ANDA040610
Manufacturer	REMEDYREPACK INC.
Substance Name	PHENYTOIN
Strength	125
Strength Unit	mg/5mL
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]