Structure (9faf1be0 1f13 47c0 B2aa 3ad62e5037e9 01)
Tolterodine Tartrate Tablet
Product Images NDC 29300-240
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 29300-240). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Unichem 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.
Company Logo (9faf1be0 1f13 47c0 B2aa 3ad62e5037e9 02)
Company Logo (9faf1be0 1f13 47c0 B2aa 3ad62e5037e9 03)
Tolterodine Tartrate Tablets 1 mg 60t (9faf1be0 1f13 47c0 B2aa 3ad62e5037e9 04)
This is a description of a medication called Tolterodine Tartrate Tablets with the National Drug Code (NDC) 29300-239-16. The text also includes an expiration date (EXP) and lot number, as well as a manufacturing company, UNICHEM LABORATORIES LTD. The medication is intended for use by patients under the supervision of a pharmacist. The text also includes information for a 2D matrix for overprinting.*
Tolterodine Tartrate Tablets 2 mg 30t (9faf1be0 1f13 47c0 B2aa 3ad62e5037e9 05)
This is a label of a box of Tolterodine Tartrate Tablets, a medicine used to reduce urinary frequency and urgency in people with overactive bladders. It contains information on the manufacturer, NDC (National Drug Code), lot number and expiration date. There are 30 tablets in the box. The label instructs to print 2D Matrix, GTIN, S/N along with EXP and LOT numbers for overprinting.*
* 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.
