United States · FDA National Drug Code directory

Cabergoline

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
23155-823_3bbcf6ce-236e-4298-81b3-f02cde1f98af
Product NDC
23155-823
Form
TABLET
Composition / generic term
Cabergoline
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20220615
Source listing expiry
20261231

Source-listed ingredients

  • CABERGOLINE — .5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 8 TABLET in 1 BOTTLE (23155-823-73) · 23155-823-73

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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