METOPROLOL TARTRATE

Product NDC
50090-7567
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
METOPROLOL TARTRATE
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA200981
Marketing category
ANDA
Substance
METOPROLOL TARTRATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7567-0180 TABLET in 1 BOTTLE (50090-7567-0) 2025-05-30NoHistorical
50090-7567-160 TABLET in 1 BOTTLE (50090-7567-1) 2025-05-30NoHistorical
50090-7567-290 TABLET in 1 BOTTLE (50090-7567-2) 2025-05-30NoHistorical
50090-7567-330 TABLET in 1 BOTTLE (50090-7567-3) 2025-05-30NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
METOPROLOL TARTRATEA-S Medication Solutions2025-06-06HUMAN PRESCRIPTION DRUG LABEL1