Atenolol

Product NDC
50090-2811
11-digit product format
500902811
Labeler code
50090
Product ID
50090-2811_1c530b16-6e36-4f78-9040-a3720813df50
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
atenolol
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA073457
Marketing category
ANDA
Marketing start
1992-01-24
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
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
50VV3VW0TIATENOLOL29122-68-7ATENOLOL

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Atenolol - A-S Medication SolutionsA-S Medication Solutions2018-06-29HUMAN PRESCRIPTION DRUG LABEL6