"51079-905-19" National Drug Code (NDC)

NDC Code	51079-905-19
Package Description	25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-905-19) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (51079-905-17)
Product NDC	51079-905
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	19990501
Marketing Category Name	ANDA
Application Number	ANDA040298
Manufacturer	Mylan Institutional 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]