Metoprolol Succinate

Product NDC
63739-454
11-digit product format
637390454
Labeler code
63739
Product ID
63739-454_0a4bd7da-8dcc-4f6c-bf4f-8f0dd6b593b9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol Succinate
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
McKesson Corporation dba SKY Packaging
Application
ANDA077298
Marketing category
ANDA
Marketing start
2010-04-15
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
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63739-454-102020-07-22C16284748780-1ab0e2407-3139-f274-e053-dbdaa90a6471361cc106-6167-43e1-93af-46b3faa5cedf
63739-454-412020-07-22C16284748780-1ab0e2407-3139-f274-e053-dbdaa90a6471361cc106-6167-43e1-93af-46b3faa5cedf

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63739-454-10EA - Each63739-454aaf78692-2876-4ba0-910d-ee990210fad412013-02-13
63739-454-41EA - Each63739-4545b802a88-8438-4b86-af8f-3d85824bdda312019-06-19