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"0078-0449-05" National Drug Code (NDC)

Lotensin 100 TABLET in 1 BOTTLE (0078-0449-05)
(Novartis Pharmaceuticals Corporation)

NDC Code0078-0449-05
Package Description100 TABLET in 1 BOTTLE (0078-0449-05)
Product NDC0078-0449
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLotensin
Non-Proprietary NameBenazepril Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date19910625
End Marketing Date20160201
Marketing Category NameNDA
Application NumberNDA019851
ManufacturerNovartis Pharmaceuticals Corporation
Substance NameBENAZEPRIL HYDROCHLORIDE
Strength20
Strength Unitmg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0078-0449-05





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