Benazepril Hydrochloride

Product NDC
71335-0267
11-digit product format
713350267
Labeler code
71335
Product ID
71335-0267_80b5095b-d8b3-4b21-8ef7-97be51391ea2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Benazepril Hydrochloride
Dosage form
TABLET, COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA076118
Marketing category
ANDA
Marketing start
2014-01-01
Substance
BENAZEPRIL HYDROCHLORIDE
Active strength
40 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Benazepril Hydrochloride
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENAZEPRIL HYDROCHLORIDE40 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiN1SN99T69T
Rxcui898719

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a4484670-2869-6416-f6ff-03b1b3cbd1b0Product name220190415
55bffd21-17e1-ff02-2e8f-1f9a532b9502Product name220150320
b9fbc696-7d55-c52e-4f12-7e3d99cd2db4Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71335-0267-1Benazepril Hydrochloride30 in 1 BOTTLETABLET, COATED30103
71335-0267-2Benazepril Hydrochloride100 in 1 BOTTLETABLET, COATED100103
71335-0267-3Benazepril Hydrochloride60 in 1 BOTTLETABLET, COATED60103
71335-0267-4Benazepril Hydrochloride90 in 1 BOTTLETABLET, COATED90103

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71335-0267BENAZEPRIL HYDROCHLORIDE TABLET, COATED [BRYANT RANCH PREPACK]103Current NDC, Legacy NDC, 4 package rows20240823_08bc0034-3b33-47d8-aec2-b36535ac85a2.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
898719benazepril HCl 40 MG Oral TabletPSN08bc0034-3b33-47d8-aec2-b36535ac85a2103
898719benazepril hydrochloride 40 MG Oral TabletSCD08bc0034-3b33-47d8-aec2-b36535ac85a2103
898719BZP hydrochloride 40 MG Oral TabletSY08bc0034-3b33-47d8-aec2-b36535ac85a2103

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-0267-17133502670130 TABLET, COATED in 1 BOTTLE (71335-0267-1) 2022-02-090000-00-00NoNoCurrent
71335-0267-271335026702100 TABLET, COATED in 1 BOTTLE (71335-0267-2) 2022-02-090000-00-00NoNoCurrent
71335-0267-37133502670360 TABLET, COATED in 1 BOTTLE (71335-0267-3) 2022-02-090000-00-00NoNoCurrent
71335-0267-47133502670490 TABLET, COATED in 1 BOTTLE (71335-0267-4) 2022-02-090000-00-00NoNoCurrent