Atenolol

Product NDC
49999-178
11-digit product format
499990178
Labeler code
49999
Product ID
49999-178_e38eb140-86b6-464c-b9e0-2229afbccd2f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Atenolol
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA073026
Marketing category
ANDA
Marketing start
1991-09-17
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
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