NDC 70518-4665 – Mirabegron

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

Human Prescription Drug

Product NDC70518-4665

Product details

Brand name
Mirabegron
Generic name
Mirabegron
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA209485
Marketed since
May 22, 2026
Listing expires
December 31, 2027
Pharmacologic class
beta3-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Mirabegron →

Package NDC codes (1)

Package NDCDescriptionSince
70518-4665-090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4665-0)May 22, 2026

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