benazepril hydrochloride and hydrochlorothiazide

Product NDC
72888-221
11-digit product format
728880221
Labeler code
72888
Product ID
72888-221_4b924079-c490-67c8-e063-6394a90aa7d0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
benazepril hydrochloride and hydrochlorothiazide
Dosage form
TABLET
Route
ORAL
Labeler
Advagen Pharma Ltd
Application
NDA020033
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2024-12-05
Substance
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE
Active strength
20; 12.5 mg/1; mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
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 and hydrochlorothiazide
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENAZEPRIL HYDROCHLORIDE20 mg/1
HYDROCHLOROTHIAZIDE12.5 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii0J48LPH2TH, N1SN99T69T
Rxcui898362, 898367, 898372

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c19ec24d-2c40-4b8d-7c20-500ffa3660a1Product name320260303
1199f4b7-b537-466c-9a1c-cb09131e9f8bProduct name120251117
e1a63b6e-1877-c2c1-01a3-03ea2817aa6fProduct name320251027
b15e9aa6-d523-ca97-480e-570e0543a342Product name420251024
96816964-c075-ffa7-b7b8-d8570411a3b9Product name720250305
162cbc9d-ecc3-72ba-af9f-c76e2756ef54Product name320221207
9b303cd4-3186-2454-5706-3137e8b2dfd2Product name420221110
47fc2fe9-7afb-4be9-989d-787aaa6ad0eaProduct name120200505
a8e65197-7914-7acf-c7ec-914d53819b34Product name320190624
8b67f333-47d1-8464-7ce4-406d3dbb295fProduct name720190618
89a57420-ab44-5323-14f9-595159145f9bProduct name220190612
c27b049d-3258-48cf-ebe5-08c236ae78e2Product name320190610
a4484670-2869-6416-f6ff-03b1b3cbd1b0Product name220190415
00fc2cf9-672f-3e0b-6afa-43cbc864d058Product name420180613
15b375b1-89c7-9594-80df-5a8c8864aee0Product name320180108
a7349398-661d-d9fc-46df-7e128bbd61d9Product name520171113
1bdb87cf-9b1f-6a51-5eb7-d182aaffaa3dProduct name220170719
e0eeb018-194e-4b70-a57d-bac47a97b8eaProduct name120160825
55bffd21-17e1-ff02-2e8f-1f9a532b9502Product name220150320
ea069444-e874-4c28-833f-d2f52734ef4dProduct name120150206
041df61b-f8b6-48a6-7b67-411e1412678bProduct name120140508
0ad8bdca-888e-00da-648b-6a4de854a167Product name120140508
433a3439-b8f3-d13a-d2c8-9b221d628d60Product name120140508
59212689-39e5-a976-6d21-882d76d8079aProduct name120140508
7613b1a5-acb6-4e5e-6048-c44deeeb1212Product name120140508
78637fb0-95c8-441f-e4b4-db1274b6f956Product name120140508
b9fbc696-7d55-c52e-4f12-7e3d99cd2db4Product name120140508
df89bd47-2db4-d593-ab37-d11953fd5536Product name120140508
f151007d-265d-9fbe-857d-1d44f1cb76baProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72888-221-01benazepril hydrochloride and hydrochlorothiazide100 in 1 BOTTLETABLET1003

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72888-221-01EA - Each72888-2211b44e7e3-f1e4-48b7-9372-22850ec452d012025-12-16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72888-221BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE TABLET [ADVAGEN PHARMA LTD]1Current NDC, 1 package rows20241208_3f6e6da8-6da3-47c5-a151-e6fd7206890e.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
898362benazepril HCl 10 MG / hydroCHLOROthiazide 12.5 MG Oral TabletPSN3f6e6da8-6da3-47c5-a151-e6fd7206890e3
898367benazepril HCl 20 MG / hydroCHLOROthiazide 12.5 MG Oral TabletPSN3f6e6da8-6da3-47c5-a151-e6fd7206890e3
898372benazepril HCl 20 MG / hydroCHLOROthiazide 25 MG Oral TabletPSN3f6e6da8-6da3-47c5-a151-e6fd7206890e3
898362benazepril hydrochloride 10 MG / hydrochlorothiazide 12.5 MG Oral TabletSCD3f6e6da8-6da3-47c5-a151-e6fd7206890e3
898367benazepril hydrochloride 20 MG / hydrochlorothiazide 12.5 MG Oral TabletSCD3f6e6da8-6da3-47c5-a151-e6fd7206890e3
898372benazepril hydrochloride 20 MG / hydrochlorothiazide 25 MG Oral TabletSCD3f6e6da8-6da3-47c5-a151-e6fd7206890e3
898362benazepril hydrochloride 10 MG / HCTZ 12.5 MG Oral TabletSY3f6e6da8-6da3-47c5-a151-e6fd7206890e3
898367benazepril hydrochloride 20 MG / HCTZ 12.5 MG Oral TabletSY3f6e6da8-6da3-47c5-a151-e6fd7206890e3
898372benazepril hydrochloride 20 MG / HCTZ 25 MG Oral TabletSY3f6e6da8-6da3-47c5-a151-e6fd7206890e3
898362BZP hydrochloride 10 MG / HCTZ 12.5 MG Oral TabletSY3f6e6da8-6da3-47c5-a151-e6fd7206890e3
898367BZP hydrochloride 20 MG / HCTZ 12.5 MG Oral TabletSY3f6e6da8-6da3-47c5-a151-e6fd7206890e3
898372BZP hydrochloride 20 MG / HCTZ 25 MG Oral TabletSY3f6e6da8-6da3-47c5-a151-e6fd7206890e3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72888-221-0172888022101100 TABLET in 1 BOTTLE (72888-221-01) 100 tablet2024-12-05NoNoCurrent