Metoprolol tartrate

Product NDC
50090-0489
11-digit product format
500900489
Labeler code
50090
Product ID
50090-0489_158c80c3-3d37-4e99-bfd0-83aa559d15c0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol tartrate
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA074644
Marketing category
ANDA
Marketing start
2015-06-29
Marketing end
0000-00-00
Substance
METOPROLOL TARTRATE
Active strength
100 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-0489-0EA - Each50090-0489b78cee35-f129-4751-99dc-1feca8c458d912018-09-05
50090-0489-1EA - Each50090-0489239e605f-048e-49da-881c-fa563cbf227a12018-09-05
50090-0489-3EA - Each50090-04895cd1c87c-ffe6-4568-bb70-83234a71d55412018-09-05
50090-0489-4EA - Each50090-048908b5c47c-04be-43de-a838-4f738445cc4412018-09-05

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-0489-05009004890030 TABLET in 1 BOTTLE (50090-0489-0) 30 tablet2015-06-290000-00-00NoNoCurrent
50090-0489-15009004890160 TABLET in 1 BOTTLE (50090-0489-1) 60 tablet2016-06-290000-00-00NoNoCurrent
50090-0489-35009004890390 TABLET in 1 BOTTLE (50090-0489-3) 90 tablet2016-06-290000-00-00NoNoCurrent
50090-0489-450090048904180 TABLET in 1 BOTTLE (50090-0489-4) 180 tablet2015-06-290000-00-00NoNoCurrent