Ropinirole Tablet, Film Coated
Product Images NDC 69452-357

View Photos of 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 69452-357). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bionpharma 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

Molecular Structure (Ropinirole Hydrochlo Figure 1)

Molecular Structure (Ropinirole Hydrochlo Figure 1)
Chemical structure of ropinirole hydrochloride, showing a benzothiazole derivative with an N,N-diethylamine side chain and a ketone functional group.*
FDA Label Image

Label 0.25 mg_100s (Ropinirole Hydrochlo Figure 2)

Label 0.25 mg_100s (Ropinirole Hydrochlo Figure 2)
Ropinirole Tablets USP 0.25 mg film-coated tablets label from Bionpharma Inc. The label indicates 100 tablets per package, storage instructions between 20°C and 25°C, and safety warnings about light, moisture, and child safety. The product is distributed by Bionpharma Inc., made in India, and includes a barcode, QR code, and identifying codes.*
FDA Label Image

Label 0.5 mg_100s (Ropinirole Hydrochlo Figure 3)

Label 0.5 mg_100s (Ropinirole Hydrochlo Figure 3)
Ropinirole 0.5 mg film-coated tablets label from Bionpharma Inc. The label indicates a package of 100 oral tablets. It includes storage instructions, a note to dispense the patient information leaflet, and product identification details including NDC 69452-357-20. The label states the product is made in India and includes a barcode and GTIN.*
FDA Label Image

Label 1 mg_100s (Ropinirole Hydrochlo Figure 4)

Label 1 mg_100s (Ropinirole Hydrochlo Figure 4)
Ropinirole Tablets, USP 1 mg film-coated tablets in a 100-tablet package. The label instructs pharmacists to dispense the patient information leaflet with the product. Distributed by Bionpharma Inc., made in India. The label includes storage instructions, safety warnings, a barcode, and lot/expiration placeholders.*
FDA Label Image

Label 2 mg_100s (Ropinirole Hydrochlo Figure 5)

Label 2 mg_100s (Ropinirole Hydrochlo Figure 5)
Ropinirole Tablets USP 2 mg film-coated tablets label for a 100-tablet package by Bionpharma Inc. The label states each tablet contains ropinirole hydrochloride equivalent to 2 mg ropinirole, with storage instructions and a pharmacist dispensing notice. It includes the NDC 69452-359-20, barcode, and GTIN information. The product is made in India.*
FDA Label Image

Label 3 mg_100s (Ropinirole Hydrochlo Figure 6)

Label 3 mg_100s (Ropinirole Hydrochlo Figure 6)
Ropinirole 3 mg film-coated tablets label showing the product name, strength, dosage form, and quantity of 100 tablets. Manufactured by Bionpharma Inc., the label includes storage instructions, dosage note, and safety warnings. The label also indicates the product is for prescription use only and dispensed with patient information leaflets.*
FDA Label Image

Label 4 mg_100s (Ropinirole Hydrochlo Figure 7)

Label 4 mg_100s (Ropinirole Hydrochlo Figure 7)
The image shows a packaging label for Ropinirole Tablets, USP, 4 mg film-coated oral tablets. The label indicates the product is prescription-only, contains 100 tablets, and is distributed by Bionpharma Inc. It includes storage instructions, dosage form, manufacturing origin (India), and barcode with associated numbers.*
FDA Label Image

Label 5 mg_100s (Ropinirole Hydrochlo Figure 8)

Label 5 mg_100s (Ropinirole Hydrochlo Figure 8)
Label for Ropinirole Tablets, USP 5 mg, film-coated oral tablets by Bionpharma Inc. The label includes storage instructions, dispensing guidance, and manufacturer details. The package contains 100 tablets and indicates the product is prescription-only, made in India.*

* 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.