"30698-449-01" National Drug Code (NDC)

Lotensin 100 TABLET in 1 BOTTLE (30698-449-01)
(Validus Pharmaceuticals LLC)

NDC Code30698-449-01
Package Description100 TABLET in 1 BOTTLE (30698-449-01)
Product NDC30698-449
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLotensin
Non-Proprietary NameBenazepril Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date19910621
Marketing Category NameNDA
Application NumberNDA019851
ManufacturerValidus Pharmaceuticals LLC
Substance NameBENAZEPRIL HYDROCHLORIDE
Strength20
Strength Unitmg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]

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