METOPROLOL SUCCINATE

Product NDC
50090-5053
11-digit product format
500905053
Labeler code
50090
Product ID
50090-5053_d3b7f75d-05b6-4bd0-acc6-daee1dfffed1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol succinate
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
A-S Medication Solutions
Application
NDA019962
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2018-01-01
Marketing end
0000-00-00
Substance
METOPROLOL SUCCINATE
Active strength
100 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50090-5053-02023-02-07C16284748780-1f386c64a-1982-0266-e053-dadaa90a7c1ab0644bf9-8880-45de-a6f4-d69cf5fd2051
50090-5053-02023-01-30C16284748780-1f386c64a-1982-0266-e053-dadaa90a7c1ab0644bf9-8880-45de-a6f4-d69cf5fd2051

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50090-5053-05009050530090 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5053-0) 2020-05-190000-00-00NoNoCurrent