United States · FDA National Drug Code directory

Bromocriptine Mesylate

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
70954-978_009f6f28-14a8-4d34-a24c-b09e90572739
Product NDC
70954-978
Form
TABLET
Composition / generic term
Bromocriptine Mesylate
Labeler
ANI Pharmaceuticals, Inc.
Marketing category
NDA
Marketing start / end (source format)
20250615
Source listing expiry
20271231

Source-listed ingredients

  • BROMOCRIPTINE MESYLATE — 2.5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (70954-978-10) · 70954-978-10
  • 100 TABLET in 1 BOTTLE (70954-978-20) · 70954-978-20

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →