Ropinirole Tablet, Film Coated
Product Images NDC 10135-678

8 FDA label images from Marlex Pharmaceuticals Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Ropinirole (NDC 10135-678). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Marlex Pharmaceuticals Inc, 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

Rop0.25

Rop0.25
Ropinirole 0.25 mg film-coated tablets label from Marlex Pharmaceuticals Inc. The label states the product name, strength, quantity of 100 tablets, and prescription-only status. It includes storage instructions, dosage information to see package insert, pharmacy dispensing advice, and manufacturing details. A barcode is present on the right side.*
FDA Label Image

Rop0.5

Rop0.5
Label for Ropinirole Tablets, USP 0.5 mg oral film-coated tablets by Marlex Pharmaceuticals Inc. The label indicates the package contains 100 tablets, prescription only. It provides storage instructions and pharmacist dispensing information along with the manufacturer details in New Castle, DE.*
FDA Label Image

Rop1

Rop1
Label for Ropinirole Tablets, USP 1 mg film-coated oral tablets by Marlex Pharmaceuticals Inc. The label states it contains 100 tablets with NDC 10135-0675-01. It includes storage instructions to keep between 20° to 25°C with permitted excursions, protecting from moisture. The label also notes it is Rx only and provides handling directions for pharmacists.*
FDA Label Image

Rop2

Rop2
Label of Ropinirole 2 mg film-coated tablets by Marlex Pharmaceuticals Inc. The label includes dosage form and strength (2 mg), quantity (100 tablets), storage instructions, and a barcode. It states the tablets contain ropinirole hydrochloride equivalent to 2 mg ropinirole and provides dispensing and handling information.*
FDA Label Image

Rop3

Rop3
Label for Ropinirole 3 mg film-coated tablets by Marlex Pharmaceuticals Inc. The label shows a count of 100 tablets, with instructions for storage at 20° to 25°C, and dispensing in a light-resistant container. The label includes a barcode and states the product is for prescription use only.*
FDA Label Image

Rop4

Rop4
Ropinirole 4 mg film-coated tablets label by Marlex Pharmaceuticals Inc. The label indicates 100 tablets per container, with instructions for storage between 20°C to 25°C and protection from moisture. The product is prescription-only and includes a barcode and NDC 10135-0678-01.*
FDA Label Image

Rop5

Rop5
Packaging label for Ropinirole Tablets, USP 5 mg film-coated tablets by Marlex Pharmaceuticals Inc. The label indicates a 100 tablet count, prescription only, with storage instructions and manufacturer details. It includes the NDC number 10135-0679-01 and barcode.*
FDA Label Image

The Structural Formula For Ropinirole Tablets, Usp Are An Orally Administered Non-ergoline Dopamine Agonist. It Is The Hydrochloride Salt Of 4-[2-(dipropylamino) Ethyl]-1, 3-dihydro-2h-indol-2-one Monohydrochloride And Has An Empirical Formula Of C16h24n2o•hcl. The Molecular Weight Is 296.84 (260.38 As The Free Base). (Ropinirole 01)

The Structural Formula For Ropinirole Tablets, Usp Are An Orally Administered Non-ergoline Dopamine Agonist. It Is The Hydrochloride Salt Of 4-[2-(dipropylamino) Ethyl]-1, 3-dihydro-2h-indol-2-one Monohydrochloride And Has An Empirical Formula Of C16h24n2o•hcl. The Molecular Weight Is 296.84 (260.38 As The Free Base). (Ropinirole 01)
Chemical structure of ropinirole hydrochloride, the active ingredient in Ropinirole tablets. The image shows the molecular arrangement including nitrogen atoms, a benzene ring, and a ketone group attached to a bicyclic structure, combined with hydrochloride (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.