Atenolol

Product NDC
55700-240
11-digit product format
557000240
Labeler code
55700
Product ID
55700-240_a06bb9ee-8c03-4a77-964f-c8b13d09734e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
atenolol
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
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