Tolterodine Tartrate Capsule, Extended Release
Product Images NDC 0904-7575

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Tolterodine Tartrate (NDC 0904-7575). 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

4mg Carton Label (E4b9ef09 C750 4e35 96fc E759ba4849d8 00)

Label for Tolterodine Tartrate Extended-release capsules, 4 mg, unit dose packaging containing 30 capsules (3 x 10). The label shows the product name, strength, dosage form, NDC 0904-7575-04, and identifies Major Pharmaceuticals as the labeler. It includes directions to dispense with patient information leaflet, storage conditions, and a note that it is for prescription use only and intended for institutional use.*

FDA Label Image

2mg Carton Label (E4b9ef09 C750 4e35 96fc E759ba4849d8 01)

The label is for Tolterodine Tartrate Extended-release Capsules, USP, 2 mg strength, unit dose packaging of 30 capsules (3 x 10) by Major Pharmaceuticals. It includes prescribing and storage instructions, highlights the non-child resistant unit dose packaging for institutional use, and displays the NDC 0904-7574-04 with barcodes and distributor information.*

FDA Label Image

Tolterodine-01 (D996a5c0 Db7e 4c41 9628 A2a4f9227af4 01)

Chemical structure diagram of Tolterodine Tartrate, showing the molecular arrangement of atoms including aromatic rings, hydroxyl groups, and carboxyl groups associated with the tartrate salt form.*

* 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.