0.25 mg Ropinirole Tablet Blister (0.25 mg Blister)
Ropinirole Hydrochloride Tablet, Film Coated
Product Images NDC 60687-588
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Product Visual Gallery
This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Ropinirole Hydrochloride (NDC 60687-588). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by American Health Packaging, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
0.25 mg Ropinirole Tablets Carton (0.25 mg Carton)
This is a description of a medication with the brand name rOPINIRole. It comes in tablet form and is only available with a prescription. Each tablet contains ropinirole hydrochloride that is equivalent to 0.25 mg of ropinirole. It is recommended to refer to the package insert for complete prescribing information. It should be stored at a temperature between 20-25°C (68-77°F) with moderate excursions permitted. The package should be protected from light and moisture and kept out of reach of children. The package should not be used if the blister is damaged or broken. The product is distributed by American Health Packaging, based in Columbus Ohio.*
1 mg Ropinirole Tablet Blister (1 mg Blister)
This text appears to be a list of several batches of TOPINIRole Tablets in 1mg dosage. Each batch has a LOT number and an EXPIRY date, which are provided alongside the product name.*
1 mg Ropinirole Tablets Carton (1 mg Carton)
This text describes a drug called "Ropinirole Tablets, USP" that comes in a package containing 100 tablets. The tablets contain Ropinirole hydrachlorids and are only available with a prescription. The pharmacist is instructed to dispense the medication with a patient information leaflet for each patient. The text contains dosage information, instructions on storage, and a warning to keep the medication out of reach of children. The package should be protected from light and moisture and should not be used if the blister is torn or broken. The drug product is distributed by American Health Packaging, based in Columbus, Ohio. The National Drug Code (NDC) for this product is 60687-588-01.*
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Structural Formula (Structure)
* 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.
