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"70518-2125-1" National Drug Code (NDC)

Benazepril Hydrochloride 30 TABLET, COATED in 1 BLISTER PACK (70518-2125-1)
(REMEDYREPACK INC.)

NDC Code70518-2125-1
Package Description30 TABLET, COATED in 1 BLISTER PACK (70518-2125-1)
Product NDC70518-2125
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBenazepril Hydrochloride
Non-Proprietary NameBenazepril Hydrochloride
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20190531
Marketing Category NameANDA
Application NumberANDA076118
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/70518-2125-1





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