Tolterodine Tartrate Tablet, Film Coated
Product Images NDC 0093-0010

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Tolterodine Tartrate (NDC 0093-0010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Pharmaceuticals Usa, 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

Image 1

Chemical structure diagram of Tolterodine Tartrate, showing the molecular arrangement of the active ingredient Tolterodine with its tartrate component.*

FDA Label Image

Image 2

Label for Tolterodine Tartrate tablets, 1 mg, film-coated oral tablets. The label shows the NDC 0093-0010-06 and indicates a package size of 60 tablets. It includes dispensing instructions, storage conditions, and manufacturer information for Teva Pharmaceuticals USA, Inc. The label design features a blue and white color scheme with a section marked 'Coding Area.'*

FDA Label Image

Image 3

Label for Tolterodine Tartrate Tablets, 2 mg, oral film-coated tablets by Teva Pharmaceuticals USA, Inc. The label includes storage instructions, safety warnings, and a barcode. It states the package contains 60 tablets and instructs pharmacists to dispense with an attached patient information leaflet. The NDC number is 0093-0018-06.*

* 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.