"71872-7079-1" National Drug Code (NDC)

NDC Code	71872-7079-1
Package Description	1 VIAL in 1 BAG (71872-7079-1) / 2 mL in 1 VIAL
Product NDC	71872-7079
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Phenytoin Sodium
Non-Proprietary Name	Phenytoin Sodium
Dosage Form	INJECTION
Usage	INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date	19750716
Marketing Category Name	ANDA
Application Number	ANDA084307
Manufacturer	Medical Purchasing Solutions, LLC
Substance Name	PHENYTOIN SODIUM
Strength	50
Strength Unit	mg/mL
Pharmacy Classes	Anti-epileptic Agent [EPC], Cytochrome P450 1A2 Inducers [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inducers [MoA], Cytochrome P450 2C8 Inducers [MoA], Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 2D6 Inducers [MoA], Cytochrome P450 3A Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE]