Mirabegron For Suspension, Extended Release
Product Images NDC 67877-890

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Mirabegron (NDC 67877-890). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ascend Laboratories, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Mirabegron Carton Label (Mirabegron Cart B)

Mirabegron Carton Label (Mirabegron Cart B)
Mirabegron for Extended-Release Oral Suspension 8 mg/mL carton label by Ascend Laboratories, LLC. The 100 mL bottle contains granules equivalent to 830 mg mirabegron. The label includes preparation instructions for suspension, pharmacist dosing directions, storage recommendations, and a barcode. It also features warnings, a patient information contact, and manufacturer details for Alkem Laboratories, India.*
FDA Label Image

Mirabegron Pouch Label (Mirabegron Pouch A)

Mirabegron Pouch Label (Mirabegron Pouch A)
Label for Mirabegron for Extended-Release Oral Suspension, 8 mg/mL, featuring instructions for use and storage. The label states it is for one bottle, not child-resistant, and intended for reconstitution from granules in a pouch. It includes branding for Ascend Laboratories, LLC, the product's NDC 67877-890-88, and notes the product is made in India.*
FDA Label Image

Mirabegron-stru (Mirabegron Stru)

Mirabegron-stru (Mirabegron Stru)
Chemical structure of Mirabegron, depicting its molecular arrangement with benzene rings, hydroxyl, amine, and thiazole functional groups.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.