NDC 50090-7642 – Cabergoline

Cabergoline .5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50090-7642

Product details

Brand name
Cabergoline
Generic name
Cabergoline
Labeler
A-S Medication Solutions
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA218618
Marketed since
October 3, 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
50090-7642-08 TABLET in 1 BOTTLE (50090-7642-0)Aug 26, 2025

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