NDC 23155-823 – Cabergoline

Cabergoline .5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC23155-823

Product details

Brand name
Cabergoline
Generic name
Cabergoline
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076310
Marketed since
June 15, 2022
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
23155-823-738 TABLET in 1 BOTTLE (23155-823-73)Jun 15, 2022

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