Ropinirole Tablet, Film Coated
Product Images NDC 0904-6373

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ropinirole (NDC 0904-6373). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, 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

Df304b5a Fe8d 4d60 B180 9a5293448d73 00

Df304b5a Fe8d 4d60 B180 9a5293448d73 00
Ropinirole 1 mg film-coated tablets in a carton unit dose package from Major Pharmaceuticals. The label displays the product name prominently with strength and dosage form, a quantity of 100 tablets, and notes the prescription-only status. It includes storage instructions, manufacturer information from Alembic Pharmaceuticals, and distributor details at Major Pharmaceuticals in Livonia, MI, along with a barcode at the bottom.*
FDA Label Image

Df304b5a Fe8d 4d60 B180 9a5293448d73 01

Df304b5a Fe8d 4d60 B180 9a5293448d73 01
Label for Ropinirole tablets, USP 0.25 mg film-coated tablets by Major Pharmaceuticals. It indicates the product is prescription only, with NDC 0904-6373-61, packaged as unit dose with 100 tablets. The label includes manufacturer and distributor information for Major Pharmaceuticals and Alembic Pharmaceuticals, plus dosage and storage instructions.*
FDA Label Image

Structure (Ropinirole Str)

Structure (Ropinirole Str)
Chemical structure of ropinirole hydrochloride, showing the indoline core with a substituted amine side chain and a ketone group, representing the molecular layout of the active ingredient ropinirole HCl.*

* 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.