Tolterodine Tartrate
Product Images NDC 0904-6592

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Tolterodine Tartrate (NDC 0904-6592). 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

F0a989af B18d 4a78 B0ee Dfbb6baf775e 00

The packaging label for Tolterodine Tartrate Extended-Release Capsules by Major Pharmaceuticals shows a 4 mg dosage strength in a unit-dose format. The label highlights that the bottle contains 30 capsules, with instructions for pharmacists to dispense with a patient information sheet. Storage and handling information is included, specifying temperature conditions and container requirements. The label also notes the product is Rx only and intended for institutional use only.*

FDA Label Image

F0a989af B18d 4a78 B0ee Dfbb6baf775e 01

Label for Tolterodine Tartrate extended-release capsules, 2 mg strength, manufactured by Major Pharmaceuticals. The label indicates a unit dose pack containing 30 capsules, for Rx use only, with pharmacist instructions to dispense with patient information sheet. Storage instructions and dosage warnings are also included, along with manufacturer and distributor addresses and a barcode.*

FDA Label Image

Structure (F0077427 85f6 4e73 9dc1 499d54810ed1 01)

Chemical structure of Tolterodine Tartrate showing the molecular arrangement of its active ingredient as depicted in the image.*

FDA Label Image

Logo (F0077427 85f6 4e73 9dc1 499d54810ed1 02)

FDA Label Image

F0077427 85f6 4e73 9dc1 499d54810ed1 03

* 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.