Benazepril Hydrochloride

Product NDC
51655-617
11-digit product format
516550617
Labeler code
51655
Product ID
51655-617_494f1b73-5bac-20fb-e063-6294a90a6428
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Benazepril Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Northwind Health Company, LLC
Application
ANDA078212
Marketing category
ANDA
Marketing start
2022-09-06
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
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Benazepril Hydrochloride
Listing expiration
2027-12-31

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
51655-617-26Benazepril Hydrochloride90 in 1 BOTTLETABLET, FILM COATED903
51655-617-52Benazepril Hydrochloride30 in 1 BOTTLE, PLASTICTABLET, FILM COATED303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51655-617BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS, LLC]2Current NDC, 2 package rows20240110_f32d01db-655b-f3d0-e053-2a95a90a04f6.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
898719benazepril HCl 40 MG Oral TabletPSNf32d01db-655b-f3d0-e053-2a95a90a04f63
898719benazepril hydrochloride 40 MG Oral TabletSCDf32d01db-655b-f3d0-e053-2a95a90a04f63
898719BZP hydrochloride 40 MG Oral TabletSYf32d01db-655b-f3d0-e053-2a95a90a04f63

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
51655-617-265165506172690 TABLET, FILM COATED in 1 BOTTLE (51655-617-26) 2022-09-06NoNoCurrent
51655-617-525165506175230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-617-52) 2023-09-20NoNoCurrent