"0078-0771-01" National Drug Code (NDC)

Maxitrol 3.5 g in 1 TUBE (0078-0771-01)
(Novartis Pharmaceuticals Corporation)

NDC Code0078-0771-01
Package Description3.5 g in 1 TUBE (0078-0771-01)
Product NDC0078-0771
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMaxitrol
Non-Proprietary NameNeomycin Sulfate, Polymyxin B Sulfate And Dexamethasone
Dosage FormOINTMENT
UsageOPHTHALMIC
Start Marketing Date19720117
Marketing Category NameNDA
Application NumberNDA050065
ManufacturerNovartis Pharmaceuticals Corporation
Substance NameDEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Strength1; 3.5; 10000
Strength Unitmg/g; mg/g; [USP'U]/g
Pharmacy ClassesAminoglycoside Antibacterial [EPC], Aminoglycosides [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Polymyxin-class Antibacterial [EPC], Polymyxins [CS]

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