Pramipexole Dihydrochloride Tablet
Product Images NDC 0615-8552

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Pramipexole Dihydrochloride (NDC 0615-8552). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ncs Healthcare Of Ky, Llc Dba Vangard Labs, 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

Chemical-structure (Pramipexole 8551 8552 1)

Chemical structure diagram of pramipexole dihydrochloride, depicting its molecular framework with labeled elements including nitrogen, sulfur, and associated hydrochloride and water components.*

FDA Label Image

Logo-01 (Pramipexole 8551 8552 2)

FDA Label Image

Logo (Pramipexole 8551 8552 3)

FDA Label Image

Principal Display Panel (Pramipexole 8551 8552 4)

Pramipexole dihydrochloride Tablets 0.25 mg oral tablets packaging label. The label shows the product name, strength, and quantity of 30 tablets. It includes manufacturer Glenmark and labeler NCS HealthCare of KY, LLC dba Vangard Labs, with packaging by Vangard in Glasgow, KY. The label also contains multiple barcode strips and storage instructions.*

FDA Label Image

Principal Display Panel (Pramipexole 8551 8552 5)

Pramipexole dihydrochloride Tablets 0.5 mg label showing product name and strength, barcode, lot number, and quantity (30 tablets). Manufacturer is Glenmark; packaging by Vanguard Labs, Glasgow, KY. Label includes storage instructions and states content per tablet as 0.5 mg of pramipexole dihydrochloride. Multiple smaller labels with identical product information and barcodes are visible for institutional use.*

* 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.