Atenolol

Product NDC
0781-1506
11-digit product format
007811506
Labeler code
0781
Product ID
0781-1506_1e5460cc-8e8d-44cf-b14b-7129a0e95122
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Atenolol
Dosage form
TABLET
Route
ORAL
Labeler
Sandoz Inc
Application
ANDA073025
Marketing category
ANDA
Marketing start
1991-09-17
Marketing end
2021-12-31
Substance
ATENOLOL
Active strength
50 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
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
faf41ef3-b4b3-a29e-3b26-07c3009003bfProduct name520220517
5eb1a708-d713-e905-0a08-b103c64796f4Product name320201019

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0781-1506-01EA - Each0781-15064c2ce85a-f951-44ac-8d1a-a62e0d603a6a12012-07-24
0781-1506-10EA - Each0781-15065c625b76-c722-4b87-a86f-02ba37f2567312012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ATENOLOLACTIVE INGREDIENT50VV3VW0TIATENOLOL TABLET [READYMEDS]15
ATENOLOLACTIVE MOIETY50VV3VW0TIATENOLOL TABLET [READYMEDS]15
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UATENOLOL TABLET [READYMEDS]15
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30ATENOLOL TABLET [READYMEDS]15
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4ATENOLOL TABLET [READYMEDS]15
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2ATENOLOL TABLET [READYMEDS]15
ATENOLOLACTIVE INGREDIENT50VV3VW0TIATENOLOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
atenololACTIVE INGREDIENT50VV3VW0TIATENOLOL TABLET [CONTRACT PHARMACY SERVICES-PA]1
ATENOLOLACTIVE MOIETY50VV3VW0TIATENOLOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
atenololACTIVE MOIETY50VV3VW0TIATENOLOL TABLET [CONTRACT PHARMACY SERVICES-PA]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UATENOLOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
COLLOIDAL SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4ATENOLOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30ATENOLOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2ATENOLOL TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197380atenolol 25 MG Oral TabletPSNbfe631e8-ab7d-40d0-b42e-ed1102955c4415
197381atenolol 50 MG Oral TabletPSNbfe631e8-ab7d-40d0-b42e-ed1102955c4415
197380atenolol 25 MG Oral TabletSCDbfe631e8-ab7d-40d0-b42e-ed1102955c4415
197381atenolol 50 MG Oral TabletSCDbfe631e8-ab7d-40d0-b42e-ed1102955c4415
197379atenolol 100 MG Oral TabletPSNe6611d33-f4c7-40c4-8db8-6f43c85d444c11
197381atenolol 50 MG Oral TabletPSNe6611d33-f4c7-40c4-8db8-6f43c85d444c11
197379atenolol 100 MG Oral TabletSCDe6611d33-f4c7-40c4-8db8-6f43c85d444c11
197381atenolol 50 MG Oral TabletSCDe6611d33-f4c7-40c4-8db8-6f43c85d444c11
197381atenolol 50 MG Oral TabletPSN00478eeb-f1c8-4355-a7c3-81c340b557d81
197381atenolol 50 MG Oral TabletPSNa2d29601-21aa-4e78-a725-6c1ea982e3ac1
197381atenolol 50 MG Oral TabletSCD00478eeb-f1c8-4355-a7c3-81c340b557d81
197381atenolol 50 MG Oral TabletSCDa2d29601-21aa-4e78-a725-6c1ea982e3ac1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0781-1506-0100781150601100 TABLET in 1 BOTTLE (0781-1506-01) 100 tablet1991-09-172021-12-31NoNoCurrent
0781-1506-10007811506101000 TABLET in 1 BOTTLE (0781-1506-10) 1000 tablet1991-09-172021-12-31NoNoCurrent