NDC 59762-1005 – Cabergoline

Cabergoline .5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC59762-1005

Product details

Brand name
Cabergoline
Generic name
cabergoline
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA020664
Marketed since
September 22, 2014
Listing expires
December 31, 2027
Pharmacologic class
Ergot Derivative

Active ingredients

Uses, dosage, side effects and warnings for Cabergoline →

Package NDC codes (1)

Package NDCDescriptionSince
59762-1005-18 TABLET in 1 BOTTLE (59762-1005-1)Sep 22, 2014

Other Cabergoline products