Metoprolol Succinate

Product NDC
82804-279
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoprolol Succinate
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA216916
Marketing category
ANDA
Substance
METOPROLOL SUCCINATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
82804-279-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82804-279-90) 2026-04-13NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Metoprolol SuccinateProficient Rx LP2026-04-01HUMAN PRESCRIPTION DRUG LABEL1