Pramipexole Dihydrochloride Tablet
Product Images NDC 0904-6704

4 FDA label images from Major Pharmaceuticals · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Pramipexole Dihydrochloride (NDC 0904-6704). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, 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

270101e8 7888 4a87 B0a8 70ebc42d2964 01

270101e8 7888 4a87 B0a8 70ebc42d2964 01
Chemical structure of pramipexole dihydrochloride monohydrate, showing the molecular arrangement of the active ingredient pramipexole with hydrochloride and water molecules.*
FDA Label Image

270101e8 7888 4a87 B0a8 70ebc42d2964 02

FDA Label Image

270101e8 7888 4a87 B0a8 70ebc42d2964 03

FDA Label Image

Image 01

Image 01
The packaging label for Pramipexole Dihydrochloride tablets, 0.25 mg strength, unit dose form. It is labeled for oral use and distributed by Major Pharmaceuticals. The label indicates a package size of 100 tablets and includes the product NDC 0904-6704-61. Manufacturer details show Torrent Pharmaceuticals Ltd. and Torrent Pharma Inc. Storage and dispensing instructions are provided, along with a barcode at the bottom.*

* 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.