"70518-3528-0" National Drug Code (NDC)

Benazepril Hydrochloride 90 TABLET in 1 BOTTLE, PLASTIC (70518-3528-0)
(REMEDYREPACK INC.)

NDC Code70518-3528-0
Package Description90 TABLET in 1 BOTTLE, PLASTIC (70518-3528-0)
Product NDC70518-3528
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBenazepril Hydrochloride
Non-Proprietary NameBenazepril Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20220920
Marketing Category NameANDA
Application NumberANDA076820
ManufacturerREMEDYREPACK 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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