Metoprolol Succinate

Product NDC
82804-014
11-digit product format
828040014
Labeler code
82804
Product ID
82804-014_502653e6-1971-4abf-9b21-ba0a9957672b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol Succinate
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA207206
Marketing category
ANDA
Marketing start
2022-04-27
Substance
METOPROLOL TARTRATE
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
W5S57Y3A5LMETOPROLOL TARTRATE56392-17-7METOPROLOL TARTRATE
TH25PD4CCBMETOPROLOL SUCCINATE98418-47-4Metoprolol Succinate

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
82804-014-308280400143030 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-014-30) 2023-10-03NoNoHistorical
82804-014-608280400146060 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-014-60) 2023-10-03NoNoHistorical
82804-014-908280400149090 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-014-90) 2023-10-03NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Metoprolol SuccinateProficient Rx LP2023-10-01HUMAN PRESCRIPTION DRUG LABEL1