Metoprolol Succinate

Product NDC
71335-0948
11-digit product format
713350948
Labeler code
71335
Product ID
71335-0948_f3be5b47-00ca-47c4-960e-0c34c49b6fec
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol Succinate
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA076862
Marketing category
ANDA
Marketing start
2009-08-04
Marketing end
0000-00-00
Substance
METOPROLOL SUCCINATE
Active strength
25 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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-0948-171335094801100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0948-1) 2009-10-270000-00-00NoNoCurrent
71335-0948-27133509480230 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0948-2) 2009-10-270000-00-00NoNoCurrent
71335-0948-37133509480390 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0948-3) 2009-10-270000-00-00NoNoCurrent
71335-0948-471335094804120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0948-4) 2009-10-270000-00-00NoNoCurrent
71335-0948-57133509480560 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0948-5) 2009-10-270000-00-00NoNoCurrent