"35356-432-90" National Drug Code (NDC)

Benazepril Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (35356-432-90)
(Lake Erie Medical DBA Quality Care Products LLC)

NDC Code35356-432-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (35356-432-90)
Product NDC35356-432
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBenazepril Hydrochloride
Non-Proprietary NameBenazepril Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20100906
Marketing Category NameANDA
Application NumberANDA076118
ManufacturerLake Erie Medical DBA Quality Care Products LLC
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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