Olanzapine Injection, Powder, Lyophilized, For Solution
Product Images NDC 0517-0955

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Olanzapine (NDC 0517-0955). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Regent, 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.

FDA Label Image

Chemical Structure (Olanzapine For Injection 1)

Chemical structure of Olanzapine, a human prescription drug. The diagram displays the molecular arrangement including benzene, nitrogen, sulfur atoms, and methyl groups characteristic of Olanzapine.*

FDA Label Image

Container Label (Olanzapine For Injection 2)

Olanzapine 10 mg/vial injection, powder, lyophilized, for solution for intramuscular use. The sterile single-use vial is labeled for injection by American Regent, Inc. Storage instructions specify 20° to 25°C before reconstitution and to use immediately after reconstitution within 1 hour. The label includes directions to see accompanying literature for dosing and administration.*

FDA Label Image

Carton Labeling (Olanzapine For Injection 3)

Olanzapine 10 mg/vial injection, powder, lyophilized for solution, labeled for intramuscular use. The single-dose vial packaging label is from American Regent, Inc., showing the product name, strength, route, and storage instructions along with inactive ingredients and reconstitution guidance. The NDC is 0517-0955-01.*

FDA Label Image

Serialization Label (Olanzapine For Injection 4)

Label image showing a lot number 'TEST', expiration date '11 2020', a GTIN barcode, and a serial number on a white background. No proprietary name or dosage details are visible on this label.*

* 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.