Ropinirole Hydrochloride Tablet, Film Coated
Product Images NDC 43547-601

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Ropinirole Hydrochloride (NDC 43547-601). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Solco Healthcare Us, 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 (Fbcd8ab4 A623 4034 Bba8 B6554bfde4b2 01)

Chemical structure of ropinirole hydrochloride, showing a bicyclic indole-like structure with a ketone and a substituted amine group including a hydrochloride component.*

FDA Label Image

Container Label 0.25 mg (Fbcd8ab4 A623 4034 Bba8 B6554bfde4b2 02)

Ropinirole hydrochloride 0.25 mg film-coated tablets packaging label from Solco Healthcare US, LLC. The label indicates 100 tablets per container, prescription use only, and contains instructions to dispense a patient information leaflet. It includes storage and safety information, the National Drug Code (NDC) 43547-595-10, and a barcode.*

FDA Label Image

Container Label 0.5 mg (Fbcd8ab4 A623 4034 Bba8 B6554bfde4b2 03)

Label for ropinirole hydrochloride tablets USP, 0.5 mg strength, film-coated tablets for oral use. The label shows the product name ropinirole with dosage 0.5 mg and states a package quantity of 100 tablets. It includes manufacturer details for Prinston Laboratories and distributor Solco Healthcare US, LLC. Storage instructions and regulatory information including NDC 43547-596-10 are visible.*

FDA Label Image

Container Label 1 mg (Fbcd8ab4 A623 4034 Bba8 B6554bfde4b2 04)

This label panel for ropinirole hydrochloride tablets USP 1 mg provides storage instructions, dosage information references, and safety warnings. It advises storage at 20° to 25°C and use of safety closures. The label includes manufacturer and distributor details for Solco Healthcare US, LLC, patient information website, and a reminder to dispense the accompanying patient information leaflet. The panel states the package contains 100 film-coated tablets.*

FDA Label Image

Container Label 2 mg (Fbcd8ab4 A623 4034 Bba8 B6554bfde4b2 05)

Label for Ropinirole hydrochloride tablets, USP, 2 mg strength. The film-coated tablets are supplied in a package containing 100 tablets. The label includes storage instructions, manufacturer Prinston Laboratories details, distributor Solco Healthcare US, LLC, and a barcode. It also notes prescription-only status and directs pharmacists to dispense the patient information leaflet.*

FDA Label Image

Container Label 3 mg (Fbcd8ab4 A623 4034 Bba8 B6554bfde4b2 06)

Ropinirole hydrochloride 3 mg film-coated tablets packaging label for oral use. The label states 'Ropinirole Tablets, USP 3 mg' and indicates a quantity of 100 tablets. It includes storage instructions and manufacturer information for Solco Healthcare US, LLC, along with National Drug Code (NDC) 43547-599-10. The label features a blue and green design with Rx only designation.*

FDA Label Image

Container Label 4 mg (Fbcd8ab4 A623 4034 Bba8 B6554bfde4b2 07)

Ropinirole hydrochloride 4 mg film-coated tablets packaging label from Solco Healthcare US, LLC. The label includes dosage strength (4 mg), prescription status (Rx only), and package quantity (100 tablets). Additional details include storage instructions, safety warnings, manufacturer and distributor information, and a barcode.*

FDA Label Image

Container Label 5 mg (Fbcd8ab4 A623 4034 Bba8 B6554bfde4b2 08)

Label for ropinirole hydrochloride 5 mg film-coated tablets by Solco Healthcare US, LLC. The label indicates the product is prescription only with NDC 43547-601-10. It contains 100 tablets and includes storage instructions, dosage information, manufacturer and distributor details, and a barcode. The label design features blue and yellow colors with a note on a non-coating area measuring 1.50" x 0.75".*

* 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.