Ropinirole Hydrochloride Tablet, Film Coated
Product Images NDC 43547-273

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Ropinirole Hydrochloride (NDC 43547-273). 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 diagram of ropinirole hydrochloride, showing its molecular framework with a heterocyclic ring and hydrochloride component.*

FDA Label Image

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

This packaging label is for ropinirole hydrochloride tablets, USP, with a strength of 0.5 mg per tablet. The label shows the tablets are film-coated and highlights a 100 tablet count. It includes storage instructions, manufacturer information (Zhejiang Huahai Pharmaceutical Co., Ltd., China), and the distributor (Solco Healthcare US, LLC). The NDC number 43547-269-10 is displayed, and the label notes it is for prescription use only.*

FDA Label Image

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

Label for ropinirole hydrochloride tablets, USP 1 mg, film-coated oral tablets. The label indicates 100 tablets per bottle and is manufactured by Zhejiang Huahai Pharmaceutical Co., Ltd., distributed by Solco Healthcare US, LLC. The label includes storage and usage instructions, barcode, and the NDC 43547-270-10.*

FDA Label Image

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

The label for ropinirole hydrochloride tablets, USP, 2 mg strength, film-coated oral tablets. The label shows the proprietary name stylized as rOPINIRole, with a count of 100 tablets. It includes the NDC 43547-271-10 and states Rx only. The labeler is Solco Healthcare US, LLC, with manufacturing by Zhejiang Huahai Pharmaceutical Co., Ltd. The label includes storage instructions and dispensing information.*

FDA Label Image

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

Label for ropinirole hydrochloride tablets, USP, 3 mg film-coated oral tablets. The label shows NDC 43547-272-10, manufactured by Zhejiang Huahai Pharmaceutical Co., Ltd., and distributed by Solco Healthcare US, LLC. The package contains 100 tablets and includes storage instructions and cautionary statements.*

FDA Label Image

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

Ropinirole hydrochloride 4 mg film-coated tablets label showing the product name and strength prominently, marked Rx only. The label includes storage instructions at 20° to 25°C, manufacturer Zhejiang Huahai Pharmaceutical Co. Ltd, and distributor Solco Healthcare US, LLC. The package contains 100 tablets and emphasizes keeping out of reach of children.*

FDA Label Image

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

Packaging label for ropinirole hydrochloride 5 mg tablets, USP, film-coated, oral dosage form. The label indicates a package size of 100 tablets, manufactured by Zhejiang Huahai Pharmaceutical Co., Ltd, and distributed by Solco Healthcare US, LLC. It includes storage instructions, safety warnings, NDC 43547-274-10, and a website link for patient information.*

FDA Label Image

Image 01

Label for ropinirole hydrochloride 0.25 mg film-coated tablets by Solco Healthcare US, LLC. The label includes product name, strength, dosage form, and pharmacy dispensing instructions, indicating 100 tablets per container. Additional details include storage instructions, warnings, manufacturer information (Zhejiang Huahai Pharmaceutical Co., Ltd.), and a barcode.*

* 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.