Tolterodine Tartrate
Product Images NDC 59762-0170

4 FDA label images from Mylan Pharmaceuticals Inc. · 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 Tolterodine Tartrate (NDC 59762-0170). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Pharmaceuticals Inc., 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 (Tolterodine 01)

Chemical Structure (Tolterodine 01)
Chemical structure of Tolterodine Tartrate showing its molecular arrangement with aromatic rings, hydroxyl groups, and the tartrate component.*
FDA Label Image

Logo (Tolterodine 02)

FDA Label Image

Principal Display Panel (1 mg Tablet Bottle Label)

Principal Display Panel (1 mg Tablet Bottle Label)
Label for Tolterodine Tartrate tablets, 1 mg strength, containing 60 tablets. The product is distributed by Greenstone LLC, Peapack, NJ. It includes storage instructions, a barcode, and a National Drug Code (NDC) 59762-0170-6. The label also indicates the brand name Greenstone and that the medication is prescription-only (Rx only).*
FDA Label Image

Principal Display Panel (2 mg Tablet Bottle Label)

Principal Display Panel (2 mg Tablet Bottle Label)
Label for Tolterodine Tartrate tablets, 2 mg, Greenstone brand. The label states the product contains 60 tablets and is distributed by Greenstone LLC, Peapack, NJ. Storage instructions specify 25°C (77°F) with permitted excursions. Includes NDC 59762-0800-2 and barcode for scanning.*

* 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.