FDA.reportPublic FDA data

Benazepril Hydrochloride

Product NDC
33261-180
11-digit product format
332610180
Labeler code
33261
Product ID
33261-180_2e92a75c-ab99-49b1-8033-efbbcace2d68
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Benazepril Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Aidarex Pharmaceuticals LLC
Application
ANDA076820
Marketing category
ANDA
Marketing start
2010-02-02
Marketing end
0000-00-00
Substance
BENAZEPRIL HYDROCHLORIDE
Active strength
20 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
2019-12-31
Current FDA listing
Historical FDA.report record

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
33261-180-302020-01-31C16284748780-19d75b9d0-a249-f424-e053-dadaa90a57ceBenazepril Hydrochloride Tablets, USP
33261-180-902020-01-31C16284748780-19d75b9d0-a249-f424-e053-dadaa90a57ceBenazepril Hydrochloride Tablets, USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
33261-180-30Benazepril Hydrochloride30 in 1 BOTTLE, PLASTICTABLET301
33261-180-90Benazepril Hydrochloride90 in 1 BOTTLE, PLASTICTABLET901

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
33261-180-30EA - Each33261-180b47bc3c3-eed5-4bdf-b5cd-feb24b852fc212015-10-02
33261-180-90EA - Each33261-180bb2fd6be-79c7-4db2-b706-ac4f8d046a2112015-10-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BENAZEPRIL HYDROCHLORIDEACTIVE INGREDIENTN1SN99T69TBENAZEPRIL HYDROCHLORIDE TABLET [AIDAREX PHARMACEUTICALS LLC]1
BENAZEPRILATACTIVE MOIETYJRM708L703BENAZEPRIL HYDROCHLORIDE TABLET [AIDAREX PHARMACEUTICALS LLC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
33261-180BENAZEPRIL HYDROCHLORIDE TABLET [AIDAREX PHARMACEUTICALS LLC]1Legacy NDC, 2 package rows20140102_c7b69325-95ba-48bd-b88e-2190f0241337.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
898687benazepril HCl 10 MG Oral TabletPSNc7b69325-95ba-48bd-b88e-2190f02413371
898690benazepril HCl 20 MG Oral TabletPSNc7b69325-95ba-48bd-b88e-2190f02413371
898719benazepril HCl 40 MG Oral TabletPSNc7b69325-95ba-48bd-b88e-2190f02413371
898687benazepril hydrochloride 10 MG Oral TabletSCDc7b69325-95ba-48bd-b88e-2190f02413371
898690benazepril hydrochloride 20 MG Oral TabletSCDc7b69325-95ba-48bd-b88e-2190f02413371
898719benazepril hydrochloride 40 MG Oral TabletSCDc7b69325-95ba-48bd-b88e-2190f02413371
898687BZP hydrochloride 10 MG Oral TabletSYc7b69325-95ba-48bd-b88e-2190f02413371
898690BZP hydrochloride 20 MG Oral TabletSYc7b69325-95ba-48bd-b88e-2190f02413371
898719BZP hydrochloride 40 MG Oral TabletSYc7b69325-95ba-48bd-b88e-2190f02413371

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
33261-180-303326101803030 in 1 BOTTLE, PLASTICHistorical
33261-180-903326101809090 in 1 BOTTLE, PLASTICHistorical