"0078-0406-05" National Drug Code (NDC)

Lotrel 100 CAPSULE in 1 BOTTLE (0078-0406-05)
(Novartis Pharmaceuticals Corporation)

NDC Code0078-0406-05
Package Description100 CAPSULE in 1 BOTTLE (0078-0406-05)
Product NDC0078-0406
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLotrel
Non-Proprietary NameAmlodipine Besylate And Benazepril Hydrochloride
Dosage FormCAPSULE
UsageORAL
Start Marketing Date19950303
End Marketing Date20260930
Marketing Category NameNDA
Application NumberNDA020364
ManufacturerNovartis Pharmaceuticals Corporation
Substance NameAMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Strength5; 20
Strength Unitmg/1; mg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Decreased Blood Pressure [PE], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]

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