"39822-4050-3" National Drug Code (NDC)

NDC Code	39822-4050-3
Package Description	25 VIAL, SINGLE-DOSE in 1 CARTON (39822-4050-3) > 2 mL in 1 VIAL, SINGLE-DOSE (39822-4050-2)
Product NDC	39822-4050
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Phenytoin Sodium
Non-Proprietary Name	Phenytoin Sodium
Dosage Form	INJECTION, SOLUTION
Usage	INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date	20110502
Marketing Category Name	ANDA
Application Number	ANDA040573
Manufacturer	X-GEN Pharmaceuticals, Inc.
Substance Name	PHENYTOIN 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]