Ropinirole Tablet, Film Coated
Product Images NDC 71335-2793

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 71335-2793). 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 (Lbl713352793)

Label (Lbl713352793)
Label for Ropinirole Tablets, USP 0.25 mg film-coated tablets. The label indicates 30 tablets per container. It includes the NDC 71335-2793-1, and states the product is Rx only. The label is repackaged by Bryant Ranch Prepack, Inc., Burbank, CA, and manufactured by OrBion Pharmaceuticals Private Ltd. Storage instructions and warnings about sealing and child safety are also included.*
FDA Label Image

Molecular Structure (Ropinirole Hydrochlo Figure 1)

Molecular Structure (Ropinirole Hydrochlo Figure 1)
Chemical structure of ropinirole hydrochloride, showing its indole-based molecular framework with a propyl group and a hydrochloride salt component.*

* 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.