"68071-2929-9" National Drug Code (NDC)

Benazepril Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (68071-2929-9)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-2929-9
Package Description90 TABLET, FILM COATED in 1 BOTTLE (68071-2929-9)
Product NDC68071-2929
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBenazepril Hydrochloride
Non-Proprietary NameBenazepril Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20080522
Marketing Category NameANDA
Application NumberANDA078212
ManufacturerNuCare Pharmaceuticals,Inc.
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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