NDC 69238-2860 – Mirabegron

Mirabegron 25 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC69238-2860

Product details

Brand name
Mirabegron
Generic name
Mirabegron
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA218543
Marketed since
April 19, 2026
Listing expires
December 31, 2027
Pharmacologic class
beta3-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Mirabegron →

Package NDC codes (2)

Package NDCDescriptionSince
69238-2860-130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2860-1)Apr 19, 2026
69238-2860-290 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2860-2)Apr 19, 2026

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