"70518-3074-1" National Drug Code (NDC)

Benazepril Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3074-1)
(REMEDYREPACK INC.)

NDC Code70518-3074-1
Package Description90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3074-1)
Product NDC70518-3074
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBenazepril Hydrochloride
Non-Proprietary NameBenazepril Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210419
Marketing Category NameANDA
Application NumberANDA078212
ManufacturerREMEDYREPACK INC.
Substance NameBENAZEPRIL HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]

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