FDA.reportPublic FDA data

ATENOLOL

Product NDC
51655-927
11-digit product format
516550927
Labeler code
51655
Product ID
51655-927_763fdd51-7683-4ac3-9c81-fe00be8e4e31
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ATENOLOL
Dosage form
TABLET
Route
ORAL
Labeler
Northwind Pharmaceuticals, LLC
Application
ANDA077877
Marketing category
ANDA
Marketing start
2015-03-26
Marketing end
0000-00-00
Substance
ATENOLOL
Active strength
50 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag
E
Listing certified through
2018-12-31
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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51655-927-522026-01-09C16284748780-19d75b9d0-744d-f424-e053-dadaa90a57ceATENOLOL
51655-927-522020-01-31C16284748780-19d75b9d0-744d-f424-e053-dadaa90a57ceATENOLOL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ATENOLOLACTIVE INGREDIENT50VV3VW0TIATENOLOL TABLET [NORTHWIND PHARMACEUTICALS, LLC]1
ATENOLOLACTIVE MOIETY50VV3VW0TIATENOLOL TABLET [NORTHWIND PHARMACEUTICALS, LLC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51655-927ATENOLOL TABLET [NORTHWIND PHARMACEUTICALS, LLC]1Legacy NDC20150401_f4414ed2-068f-47d3-bd6d-6a2e501304a7.zip