NDC 70069-824 – Cabergoline

Cabergoline .5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70069-824

Product details

Brand name
Cabergoline
Generic name
Cabergoline
Labeler
Somerset Therapeutics, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA218109
Marketed since
October 18, 2024
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
70069-824-088 TABLET in 1 BOTTLE (70069-824-08)Oct 18, 2024

Other Cabergoline products