NDC 0093-5420 – Cabergoline

Cabergoline .5 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC0093-5420

Product details

Brand name
Cabergoline
Generic name
Cabergoline
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077750
Marketed since
March 7, 2007
Listing expires
December 31, 2026
Pharmacologic class
Ergot Derivative

Active ingredients

Uses, dosage, side effects and warnings for Cabergoline →

Package NDC codes (1)

Package NDCDescriptionSince
0093-5420-881 BOTTLE in 1 CARTON (0093-5420-88) / 8 TABLET in 1 BOTTLEMar 7, 2007

Recalls mentioning this NDC

Other Cabergoline products