NDC 68180-151 – Mirabegron

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

Human Prescription Drug

Product NDC68180-151

Product details

Brand name
Mirabegron
Generic name
Mirabegron
Labeler
Lupin Pharmaceuticals, Inc.
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 (2)

Package NDCDescriptionSince
68180-151-0630 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68180-151-06)Apr 19, 2024
68180-151-0990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68180-151-09)Apr 19, 2024

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