Olanzapine Tablet, Film Coated
Product Images NDC 72789-341

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Olanzapine (NDC 72789-341). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx Pharmaceuticals, 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

72789341 Label (72789341)

Label for Olanzapine USP 20 mg film-coated tablets by PD-Rx Pharmaceuticals, Inc. The label shows package details including 90 tablets, NDC 72789-341-90, expiration date 09/2027, and lot number H23A23. It includes safety warnings, dosing instructions, and a QR code. The label is white with black text and purple branding elements.*

FDA Label Image

138 (Olanzapine Tab Str)

Chemical structure diagram of olanzapine showing its molecular framework with nitrogen, sulfur atoms, and methyl groups as part of its heterocyclic system.*

* 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.