Benazepril Hydrochloride

Product NDC
0185-0820
11-digit product format
001850820
Labeler code
0185
Product ID
0185-0820_0d6a5892-753f-4b12-bb9a-a2a99937b6e3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Benazepril Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Eon Labs, Inc.
Application
ANDA076402
Marketing category
ANDA
Marketing start
2004-02-11
Marketing end
2021-10-31
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
0000-00-00
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0185-0820-01EA - Each0185-0820ac3c3d7a-2a8e-4ce5-99d7-fa48a9205e9a12012-07-24
0185-0820-05EA - Each0185-082043b09963-b6f8-4e70-9605-3dc55229859e12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
benazepril hydrochlorideACTIVE INGREDIENTN1SN99T69TBENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.]1
D&C YELLOW NO. 10ACTIVE INGREDIENT35SW5USQ3GBENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.]1
benazeprilACTIVE MOIETYUDM7Q7QWP8BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UBENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.]1
colloidal silicon dioxideINACTIVE INGREDIENTETJ7Z6XBU4BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.]1
crospovidoneINACTIVE INGREDIENT68401960MKBENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.]1
D&C YELLOW NO. 10INACTIVE INGREDIENT35SW5USQ3GBENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.]1
FD&C RED NO. 40INACTIVE INGREDIENTWZB9127XOABENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.]1
FD&C YELLOW NO. 6INACTIVE INGREDIENTH77VEI93A8BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.]1
HYDROGENATED CASTOR OILINACTIVE INGREDIENTZF94AP8MEYBENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.]1
hypromelloseINACTIVE INGREDIENT3NXW29V3WOBENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.]1
lactose monohydrateINACTIVE INGREDIENTEWQ57Q8I5XBENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.]1
polyethylene glycolINACTIVE INGREDIENT3WJQ0SDW1ABENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.]1
POLYSORBATE 20INACTIVE INGREDIENT7T1F30V5YHBENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.]1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJBENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.]1
titanium dioxideINACTIVE INGREDIENT15FIX9V2JPBENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.]1
zinc stearateINACTIVE INGREDIENTH92E6QA4FVBENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.]1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
898690benazepril HCl 20 MG Oral TabletPSN56ffd662-60a6-4b43-a7ea-f778714dfbbd1
898719benazepril HCl 40 MG Oral TabletPSN56ffd662-60a6-4b43-a7ea-f778714dfbbd1
898723benazepril HCl 5 MG Oral TabletPSN56ffd662-60a6-4b43-a7ea-f778714dfbbd1
898690benazepril hydrochloride 20 MG Oral TabletSCD56ffd662-60a6-4b43-a7ea-f778714dfbbd1
898719benazepril hydrochloride 40 MG Oral TabletSCD56ffd662-60a6-4b43-a7ea-f778714dfbbd1
898723benazepril hydrochloride 5 MG Oral TabletSCD56ffd662-60a6-4b43-a7ea-f778714dfbbd1
898723benazepril HCl 5 MG Oral TabletSY56ffd662-60a6-4b43-a7ea-f778714dfbbd1
898690BZP hydrochloride 20 MG Oral TabletSY56ffd662-60a6-4b43-a7ea-f778714dfbbd1
898719BZP hydrochloride 40 MG Oral TabletSY56ffd662-60a6-4b43-a7ea-f778714dfbbd1
898723BZP hydrochloride 5 MG Oral TabletSY56ffd662-60a6-4b43-a7ea-f778714dfbbd1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0185-0820-0100185082001100 TABLET, FILM COATED in 1 BOTTLE (0185-0820-01) 2004-02-112021-10-31NoNoCurrent
0185-0820-0500185082005500 TABLET, FILM COATED in 1 BOTTLE (0185-0820-05) 2004-02-112021-10-31NoNoCurrent