Atenolol

Product NDC
16571-441
11-digit product format
165710441
Labeler code
16571
Product ID
16571-441_d5072024-c824-4740-93af-02340db518ff
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Atenolol
Dosage form
TABLET
Route
ORAL
Labeler
Pack Pharmaceuticals LLC
Application
ANDA077443
Marketing category
ANDA
Marketing start
2010-06-10
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
16571-441-112024-03-05C16284748780-19d75b9d1-15d2-f424-e053-dadaa90a57ce8c137b74-6a28-4760-b8d5-f453efa95a9e
16571-441-112020-01-31C16284748780-19d75b9d1-15d2-f424-e053-dadaa90a57ce8c137b74-6a28-4760-b8d5-f453efa95a9e

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
16571-441-11EA - Each16571-4418b2937d5-2571-4e3b-8fc2-bb69875ea57812012-07-24