Carvedilol

Product NDC
50090-6865
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Carvedilol
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA078251
Marketing category
ANDA
Substance
CARVEDILOL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6865-090 TABLET, FILM COATED in 1 BOTTLE (50090-6865-0) 2023-12-04NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
CarvedilolA-S Medication Solutions2023-12-05HUMAN PRESCRIPTION DRUG LABEL1