Metoprolol Succinate

Product NDC
50090-6448
11-digit product format
500906448
Labeler code
50090
Product ID
50090-6448_d30564b1-14c8-4a83-9925-b81a743d8485
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol Succinate
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
A-S Medication Solutions
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
50090-6448-05009064480030 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6448-0) 2023-04-26NoNoHistorical
50090-6448-15009064480190 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6448-1) 2023-04-26NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Metoprolol SuccinateA-S Medication Solutions2023-04-30HUMAN PRESCRIPTION DRUG LABEL1