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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49999-178-00EA - Each49999-1786199a9ff-e94f-4cbe-b26f-02f0d689025512015-06-09
49999-178-30EA - Each49999-178468ac241-52e5-4bab-8a34-213d54df3f8012015-06-09
49999-178-60EA - Each49999-178b83743c2-1b93-4a8b-a7d5-21524578cb5512015-06-09
49999-178-90EA - Each49999-1781552791c-2db1-4e94-955a-cafc23ecffd012015-06-09