Tolterodine Tartrate Capsule, Extended Release
Product Images NDC 13668-190

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Tolterodine Tartrate (NDC 13668-190). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Torrent Pharmaceuticals Limited, 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

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

Structure (F0077427 85f6 4e73 9dc1 499d54810ed1 01)
Chemical structure of Tolterodine Tartrate, an active pharmaceutical ingredient in human prescription drugs. The image shows the molecular formula depicting the Tolterodine molecule bonded with tartaric acid, representing its tartrate salt form.*
FDA Label Image

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

FDA Label Image

Torrent Logo (F0077427 85f6 4e73 9dc1 499d54810ed1 03)

FDA Label Image

Label 2mg (F0077427 85f6 4e73 9dc1 499d54810ed1 04)

Label 2mg (F0077427 85f6 4e73 9dc1 499d54810ed1 04)
Label for Tolterodine Tartrate Extended-Release Capsules 2 mg, containing 30 capsules per bottle. The label includes storage instructions, dosage form, strength, manufacturer details (Torrent Pharmaceuticals Limited), NDC 13668-189-30, and a barcode. The label notes it is a prescription drug and advises dispensing the patient information sheet with each prescription.*
FDA Label Image

Label 4mg (F0077427 85f6 4e73 9dc1 499d54810ed1 05)

Label 4mg (F0077427 85f6 4e73 9dc1 499d54810ed1 05)
Label for Tolterodine Tartrate Extended-Release Capsules 4 mg, containing 30 capsules. The label includes storage instructions, dosage directions referencing prescribing information, and manufacturing details by Torrent Pharmaceuticals Ltd. It features a barcode, NDC 13668-190-30, and states Rx only. The label also instructs pharmacists to dispense a patient information sheet with each prescription.*

* 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.