"70934-983-30" National Drug Code (NDC)

Benazepril Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-983-30)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-983-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-983-30)
Product NDC70934-983
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBenazepril Hydrochloride
Non-Proprietary NameBenazepril Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220628
End Marketing Date20231231
Marketing Category NameANDA
Application NumberANDA078212
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance NameBENAZEPRIL HYDROCHLORIDE
Strength40
Strength Unitmg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]

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