"10139-025-22" National Drug Code (NDC)

NDC Code	10139-025-22
Package Description	10 VIAL, SINGLE-DOSE in 1 CARTON (10139-025-22) > 10 mL in 1 VIAL, SINGLE-DOSE (10139-025-12)
Product NDC	10139-025
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Fosphenytoin Sodium
Non-Proprietary Name	Fosphenytoin Sodium
Dosage Form	INJECTION, SOLUTION
Usage	INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date	20070806
Marketing Category Name	ANDA
Application Number	ANDA078277
Manufacturer	GeneraMedix Inc.
Substance Name	FOSPHENYTOIN SODIUM
Strength	50
Strength Unit	mg/mL
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]