Atenolol

Product NDC
53217-201
11-digit product format
532170201
Labeler code
53217
Product ID
53217-201_c15d4c91-c662-49c6-ade5-0c7ccdf4d761
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Atenolol
Dosage form
TABLET
Route
ORAL
Labeler
Aidarex Pharmaceuticals LLC
Application
ANDA074056
Marketing category
ANDA
Marketing start
1995-02-22
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 TABLETS USP 0787 0752 0753 Rx onlyAidarex Pharmaceuticals LLC2017-03-01HUMAN PRESCRIPTION DRUG LABEL1