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"70518-3171-0" National Drug Code (NDC)

Benazepril Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3171-0)
(REMEDYREPACK INC.)

NDC Code70518-3171-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3171-0)
Product NDC70518-3171
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBenazepril Hydrochloride
Non-Proprietary NameBenazepril Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210726
Marketing Category NameANDA
Application NumberANDA078212
ManufacturerREMEDYREPACK INC.
Substance NameBENAZEPRIL HYDROCHLORIDE
Strength40
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/70518-3171-0





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