"51655-202-26" National Drug Code (NDC)

Benazepril Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-202-26)
(Northwind Pharmaceuticals, LLC)

NDC Code51655-202-26
Package Description90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-202-26)
Product NDC51655-202
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBenazepril Hydrochloride
Non-Proprietary NameBenazepril Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20230315
Marketing Category NameANDA
Application NumberANDA078212
ManufacturerNorthwind Pharmaceuticals, LLC
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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