United States · FDA National Drug Code directory

Mirabegron

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
69238-2860_0bfa52f0-d4b2-4fb1-b3ee-da4cba2b18fd
Product NDC
69238-2860
Form
TABLET, FILM COATED, EXTENDED RELEASE
Composition / generic term
Mirabegron
Labeler
Amneal Pharmaceuticals NY LLC
Marketing category
ANDA
Marketing start / end (source format)
20260419
Source listing expiry
20271231

Source-listed ingredients

  • MIRABEGRON — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2860-1) · 69238-2860-1
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2860-2) · 69238-2860-2

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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