Ropinirole Hydrochloride
Product Images NDC 64220-420

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Ropinirole Hydrochloride (NDC 64220-420). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zhejiang Huahai Pharmaceutical Co., Ltd., 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 Of Ropinirole HCl (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 01)

Chemical structure of Ropinirole Hydrochloride showing its molecular arrangement including the indole core and associated functional groups as depicted in the image.*

FDA Label Image

Ropinirole HCl 0.25mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 05)

Label for Ropinirole Hydrochloride Tablets 0.25 mg, containing 100 tablets. The label shows the NDC number 64220-420-01 and indicates prescription only use. It includes storage instructions, manufacturer Zhejiang Huahai Pharmaceutical Co., Ltd., and barcode. The label also advises dispensing a patient information leaflet with each prescription.*

FDA Label Image

Ropinirole HCl 0.5mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 06)

Ropinirole Hydrochloride Tablets 0.5 mg label from Zhejiang Huahai Pharmaceutical Co., Ltd. The package contains 100 tablets. The label includes storage instructions, safety warnings, dispenser instructions, and manufacturer information. The NDC number 64220-421-01 and a barcode are also visible.*

FDA Label Image

Ropinirole HCl 1mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 07)

Label for Ropinirole Hydrochloride Tablets 1 mg, showing 100 tablets per bottle. The label includes storage instructions to keep at 20° to 25°C, warnings to keep out of reach of children, and directions for pharmacists to dispense the accompanying patient information leaflet. Manufactured by Zhejiang Huahai Pharmaceutical Co., Ltd.*

FDA Label Image

Ropinirole HCl 2mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 08)

Ropinirole Hydrochloride Tablets 2 mg label showing NDC 64220-423-01. The label indicates a package containing 100 tablets, Rx only. It includes storage instructions and manufacturer details for Zhejiang Huahai Pharmaceutical Co., Ltd. The label also notes dispensing instructions and a barcode.*

FDA Label Image

Ropinirole HCl 3mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 09)

Label for Ropinirole Hydrochloride Tablets 3 mg, containing 100 tablets. The label includes the NDC number 64220-424-01 and storage instructions to keep at 20 to 25°C, protected from light and moisture. It states Rx only and is manufactured by Zhejiang Huahai Pharmaceutical Co., Ltd. The label includes a barcode and a reminder to dispense the accompanying patient information leaflet.*

FDA Label Image

Ropinirole HCl 4mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 10)

Label for Ropinirole Hydrochloride Tablets 4 mg, containing 100 tablets. The label includes NDC code 64220-425-01 and specifies dispensing only by prescription. Instructions note storage at 20° to 25°C with protection from light and moisture. The product is manufactured by Zhejiang Huahai Pharmaceutical Co., Ltd., Linhai, Zhejiang, China, for Prinston Pharmaceutical Inc., Cranbury, NJ USA.*

FDA Label Image

Ropinirole HCl 5mg Label (Db5b7681 1e06 4ff2 A0c1 5304b298f0f0 11)

Label for Ropinirole Hydrochloride Tablets 5 mg, packaging of 100 tablets for prescription use only. Manufactured by Zhejiang Huahai Pharmaceutical Co., Ltd. The label includes storage instructions to keep at 20 to 25°C and warnings to keep out of reach of children. Barcode and spaces for lot and expiration information are visible.*

* 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.