Atenolol

Product NDC
55700-243
11-digit product format
557000243
Labeler code
55700
Product ID
55700-243_1fcc3c18-0eee-4378-873f-461d41d9a7fb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Atenolol
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA073025
Marketing category
ANDA
Marketing start
1991-09-17
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55700-243-30EA - Each55700-243da510277-919c-4ff8-870f-05666813d1a312016-12-07
55700-243-60EA - Each55700-243b0725b78-348f-4acf-b9f1-e4764e298c9a12016-12-07
55700-243-90EA - Each55700-243150c60aa-47a3-4d08-9659-5f778b7dc2bd12016-12-07