Ropinirole Hydrochloride Tablet, Film Coated
Product Images NDC 51655-360

2 FDA label images from Northwind Health Company, Llc · 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 Hydrochloride (NDC 51655-360). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, 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

Label (51655 360 26 Master Bottle Label Approval Rev A 05 20)

Label (51655 360 26 Master Bottle Label Approval   Rev A 05 20)
Label for ropinirole hydrochloride 0.25 mg film-coated tablets, oral route, supplied in a bottle containing 90 tablets. The label states the product is prescription only, with storage instructions at 20 to 25°C, and warnings to keep out of reach of children and protect from light and moisture. The labeler is Northwind Health Company, LLC, with product NDC 51655-360-26.*
FDA Label Image

Structural Formula (Fbcd8ab4 A623 4034 Bba8 B6554bfde4b2 01)

Structural Formula (Fbcd8ab4 A623 4034 Bba8 B6554bfde4b2 01)
Chemical structure of ropinirole hydrochloride depicted as a molecular diagram showing its chemical bonds and 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.