"49349-355-02" National Drug Code (NDC)

NDC Code	49349-355-02
Package Description	30 CAPSULE in 1 BLISTER PACK (49349-355-02)
Product NDC	49349-355
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Dilantin
Non-Proprietary Name	Phenytoin Sodium
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20110708
Marketing Category Name	ANDA
Application Number	ANDA084349
Manufacturer	REMEDYREPACK INC.
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]