Metoprolol Succinate

Product NDC
71610-642
11-digit product format
716100642
Labeler code
71610
Product ID
71610-642_2d0c7cc9-b09e-4014-809e-c9e30ab481ca
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol Succinate
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA204106
Marketing category
ANDA
Marketing start
2018-02-06
Substance
METOPROLOL SUCCINATE
Active strength
50 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
TH25PD4CCBMETOPROLOL SUCCINATE98418-47-4METOPROLOL SUCCINATE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
71610-642-457161006424545 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-642-45) 2022-03-29NoNoHistorical
71610-642-537161006425360 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-642-53) 2022-03-29NoNoHistorical
71610-642-607161006426090 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-642-60) 2022-03-29NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Metoprolol SuccinateAphena Pharma Solutions - Tennessee, LLC2022-03-29HUMAN PRESCRIPTION DRUG LABEL1