FDA.reportPublic FDA data

Atenolol

Product NDC
35356-930
11-digit product format
353560930
Labeler code
35356
Product ID
35356-930_34da6242-0058-4a6d-8a60-8cfe52b28c34
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Atenolol
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA074052
Marketing category
ANDA
Marketing start
1992-05-01
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 Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
35356-930-30EA - Each35356-930e2181238-b21b-4e59-960c-820f745bcf7712013-09-04
35356-930-60EA - Each35356-930116b9c13-fa0c-4e2c-9ddb-98844cbd6fa012013-09-04
35356-930-90EA - Each35356-930e44f49a5-e070-4424-a9ff-36b9df5db91012013-09-04