Atenolol

Product NDC
0615-3533
11-digit product format
006153533
Labeler code
0615
Product ID
0615-3533_2c9479d8-ddb7-4d42-93bb-cdc7be1ba8b1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
atenolol
Dosage form
TABLET
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA073457
Marketing category
ANDA
Marketing start
2012-04-30
Marketing end
0000-00-00
Substance
ATENOLOL
Active strength
100 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0615-3533-392021-03-08C16284748780-19d75b9d0-a258-f424-e053-dadaa90a57ce0031ae52-111e-4f6d-9a1c-3e85ea233418
0615-3533-392020-01-31C16284748780-19d75b9d0-a258-f424-e053-dadaa90a57ce0031ae52-111e-4f6d-9a1c-3e85ea233418