NDC 71335-2810 – Mirabegron

Mirabegron 50 mg/1 · Tablet, Film Coated, Extended Release · Oral

Human Prescription Drug

Product NDC71335-2810

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
September 3, 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
71335-2810-190 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2810-1)Sep 26, 2025

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