Cabergoline

Product NDC
50090-6596
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cabergoline
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA076310
Marketing category
ANDA
Substance
CABERGOLINE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6596-08 TABLET in 1 BOTTLE (50090-6596-0) 2023-08-18NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
CABERGOLINE TABLETS, USP Rx onlyA-S Medication Solutions2023-08-28HUMAN PRESCRIPTION DRUG LABEL1