NDC 71335-2807 – Mirabegron

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

Human Prescription Drug

Product NDC71335-2807

Product details

Brand name
Mirabegron
Generic name
mirabegron
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA209485
Marketed since
April 19, 2024
Listing expires
December 31, 2026
Pharmacologic class
beta3-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Mirabegron →

Package NDC codes (1)

Package NDCDescriptionSince
71335-2807-11 BOTTLE in 1 CARTON (71335-2807-1) / 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLESep 26, 2025

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