Detrol La
Product Images NDC 58151-103

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Detrol La (NDC 58151-103). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Viatris Specialty Llc, 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

Detrol La Bottle Label 2 mg (Image 01)

Detrol La Bottle Label 2 mg (Image 01)
Label for Detrol LA 2 mg extended release capsules containing tolterodine tartrate. The carton indicates 30 capsules per package and is labeled Rx only. Distributed by Viatris Specialty LLC. Storage instructions note to store at 25°C with permitted excursions from 15-30°C and to protect from light. The Viatris logo is present on the label.*
FDA Label Image

Detrol La Bottle Label 4 mg (Image 02)

Detrol La Bottle Label 4 mg (Image 02)
Label for Detrol LA 4 mg extended release capsules containing tolterodine tartrate. The package includes 30 capsules and is labeled for prescription use only. The label shows storage instructions, dosage notice, and lists Viatris Specialty LLC as the distributor located in Morgantown, WV. The design features a blue block highlighting the 4 mg strength and includes a barcode and lot information.*
FDA Label Image

Tolterodine Tartrate Structural Formula (Image 03)

Tolterodine Tartrate Structural Formula (Image 03)
Chemical structure diagram depicting the molecular structure of the active ingredient in Detrol LA by Viatris Specialty LLC. The structure shows a detailed representation of the chemical bonds and functional groups present.*

* 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.