Ropinirole Hydrochloride
Product Images NDC 53217-166

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Ropinirole Hydrochloride (NDC 53217-166). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aidarex Pharmaceuticals 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

Formula (Ropinirole Heritage 1)

Chemical structure depicting the molecular composition of ropinirole hydrochloride, highlighting the indole core and associated functional groups as part of its formulation.*

FDA Label Image

Company Logo (Ropinirole Heritage 2)

FDA Label Image

Logo (Ropinirole Heritage 3)

FDA Label Image

Logo (Ropinirole Heritage 4)

FDA Label Image

Display Image (Ropinirole Heritage 5)

Ropinirole Hydrochloride 0.25 MG film-coated tablets packaging label showing 30 tablets. The label includes drug name ROPINIROLE USP 0.25MG, dosage form as film-coated tablets, active ingredient listed as Ropinirole Hydrochloride USP equivalent to 0.25 mg Ropinirole free base. Labeler is Aidarex Pharmaceuticals LLC with manufacturing by Heritage Pharmaceuticals Inc., Edison, NJ. The label also displays NDC 53217-0166-30 and dosing instructions space in English and Spanish.*

* 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.