Ropinirole
Product Images NDC 43353-920

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Ropinirole (NDC 43353-920). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, 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

Structural Formula (35e65939 Fe12 49d0 Bdb3 Bf08690f7c59 01)

Chemical structure of ropinirole hydrochloride, showing its distinct fused ring and side chain features typical for this active ingredient.*

FDA Label Image

Bottle Label 2mg (43353 911)

Label for Ropinirole 2 mg tablets, containing 9000 tablets. The label indicates storage instructions, manufacturer Roxane Laboratories in Columbus, OH, and repackaging by Aphena Pharma Solutions - Tennessee, LLC in Cookeville, TN. It is marked RX Only and includes barcodes and batch/lot fields.*

FDA Label Image

Bottle Label 1mg (43353 912)

Label for Ropinirole 1 mg tablets, containing 9000 tablets. The label indicates storage between 20-25 degrees Celsius and dispensing in a light-resistant container. Manufactured by Roxane Laboratories in Columbus, OH, and repackaged by Aphena Pharma Solutions - Tennessee, LLC, Cookeville, TN. The product is marked RX only.*

FDA Label Image

Bottle Label 0.25mg (43353 920)

Label for Ropinirole 0.25 mg tablets containing 9000 tablets. The label indicates storage instructions, manufacturer Roxane Laboratories in Columbus, OH, and repackaging by Aphena Pharma Solutions - Tennessee, LLC in Cookeville, TN. The label also includes NDC 43353-0920-09 and notes RX Only.*

FDA Label Image

Aphena Pharma Solutions (TN)

* 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.