Ziprasidone Mesylate Injection, Powder, Lyophilized, For Solution
Product Images NDC 68083-340

3 FDA label images from Gland Pharma Limited · 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 Ziprasidone Mesylate (NDC 68083-340). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gland Pharma 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

Zipra Spl Carton Label

Zipra Spl Carton Label
Packaging label for Ziprasidone Mesylate for Injection 20 mg/mL, a lyophilized powder for intramuscular injection. The label shows it is a single-dose sterile vial, Rx only, manufactured by Gland Pharma Limited, Hyderabad, India. Storage instructions indicate 20°C to 25°C with light protection. The label includes reconstitution instructions and dosage information.*
FDA Label Image

Zipra Spl Container Label

Zipra Spl Container Label
Label for Ziprasidone Mesylate for Injection, 20 mg/mL, lyophilized powder for intramuscular use. It is a single-dose vial, sterile, and Rx only. Instructions include reconstitution with 1.2 mL sterile water for injection and storage at 20°C to 25°C. The label also notes protection from light and that the solution turns colorless to pale pink when dissolved. Manufactured by Gland Pharma Limited, India.*
FDA Label Image

Zipra Spl Structure

Zipra Spl Structure
Chemical structure diagram of the active ingredient ziprasidone mesylate, showing its molecular framework and arrangement of atoms.*

* 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.