Tizanidine Tablet
Product Images NDC 35356-662

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Tizanidine (NDC 35356-662). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Quality Care Products, 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

Image Description (Tizanidinehcl2mg)

This is a warning label and prescription information for Tizanidine tablets manufactured by Dr. Reddy's Laboratories Limited in India. It includes a caution to keep the medication away from children, recommended storage temperature, dosage information, and manufacturer details.*

FDA Label Image

Image Description (Fig1)

This text shows a table that lists the concentration of Tzanidine, a medication, in plasma after different dosages of 4 mg tablets or capsules taken with or without food. The concentration values are given in ng/mL, and the time since dosing is given in hours.*

FDA Label Image

Image Description (Fig2)

The text is a graph or chart, and the has failed to recognize the labels and values present, making it not-available for generating a useful description.*

FDA Label Image

Image Description (Fig3)

This text is describing a study that evaluated the improvement in Ashworth Score, a measure of muscle spasticity, in individuals taking a medication called Zanidine. The mean dose of Zanidine administered was 28.6 mg. The study lasted for 7 weeks, with the endpoint being the end of the maintenance phase. The last observation carried forward method was used to analyze the results.*

FDA Label Image

Image Description (Structure)

* 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.