FDA.reportPublic FDA data

Atenolol

Product NDC
51655-926
11-digit product format
516550926
Labeler code
51655
Product ID
51655-926_1937395b-5f4b-4e04-ae88-d60909220cf1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Atenolol
Dosage form
TABLET
Route
ORAL
Labeler
Northwind Pharmaceuticals, LLC
Application
ANDA077877
Marketing category
ANDA
Marketing start
2014-06-24
Marketing end
0000-00-00
Substance
ATENOLOL
Active strength
25 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2019-12-31
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
51655-926-522026-01-09C16284748780-19d75b9d0-46a2-f424-e053-dadaa90a57ceAtenolol 25 MG
51655-926-522020-01-31C16284748780-19d75b9d0-46a2-f424-e053-dadaa90a57ceAtenolol 25 MG

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
51655-926ATENOLOL TABLET [NORTHWIND PHARMACEUTICALS, LLC]1Legacy NDC20140724_f23be9b8-5dd0-4025-99b1-6dcf8e14b185.zip