Ropinirole Tablet, Film Coated
Product Images NDC 72162-2200

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ropinirole (NDC 72162-2200). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Label (Lbl721622200)

Label (Lbl721622200)
This is a description for a medication called rOPINIRole Tablets, USP. Each film-coated tablet contains 0.5 mg of Ropinirole Hydrochloride, which is used for a specific medical purpose. It is important to keep this medication out of reach of children and protect it from light and moisture. The tablets should be stored at a temperature between 20° to 25°C (68° to 77°F). This medication is dispensed with patient package inserts, and safety closures should be used unless otherwise directed by a physician. The NDC number for this product is 72162-2200-1. The tablets are manufactured by Bryant Ranch Prepack, Inc. and relabeled by OrBion Pharmaceuticals.*
FDA Label Image

Molecular Structure (Ropinirole Hydrochlo Figure 1)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.