"0071-0369-32" National Drug Code (NDC)

Dilantin 1000 CAPSULE in 1 BOTTLE (0071-0369-32)
(Parke-Davis Div of Pfizer Inc)

NDC Code0071-0369-32
Package Description1000 CAPSULE in 1 BOTTLE (0071-0369-32)
Product NDC0071-0369
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDilantin
Non-Proprietary NameExtended Phenytoin Sodium
Dosage FormCAPSULE
UsageORAL
Start Marketing Date19760827
Marketing Category NameANDA
Application NumberANDA084349
ManufacturerParke-Davis Div of Pfizer Inc
Substance NamePHENYTOIN SODIUM
Strength100
Strength Unitmg/1
Pharmacy ClassesAnti-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]

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