Carvedilol

Product NDC
50090-7786
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Carvedilol
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA077614
Marketing category
ANDA
Substance
CARVEDILOL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7786-090 TABLET, FILM COATED in 1 BOTTLE (50090-7786-0) 2025-11-21NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
CarvedilolA-S Medication Solutions2025-12-02HUMAN PRESCRIPTION DRUG LABEL8