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"23155-751-05" National Drug Code (NDC)

Benazepril Hydrochloride 500 TABLET in 1 BOTTLE (23155-751-05)
(Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)

NDC Code23155-751-05
Package Description500 TABLET in 1 BOTTLE (23155-751-05)
Product NDC23155-751
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBenazepril Hydrochloride
Non-Proprietary NameBenazepril Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20220820
Marketing Category NameANDA
Application NumberANDA076267
ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Substance NameBENAZEPRIL HYDROCHLORIDE
Strength20
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/23155-751-05





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