Olanzapine Tablet, Film Coated
Product Images NDC 55111-163

3 FDA label images from Dr. Reddy's Laboratories Ltd. · 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 Olanzapine (NDC 55111-163). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Reddy's Laboratories Ltd., 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

Carton1 (Carton1)

Carton1 (Carton1)
Packaging label for Olanzapine Tablets, USP 2.5 mg, film-coated oral tablets. The label indicates 100 tablets (10 x 10 unit-dose) per package, manufactured by Dr. Reddy's Laboratories Limited. It includes usage instructions for pharmacists and storage conditions at controlled room temperature (20° to 25°C). The label features branding and regulatory information including the NDC 55111-163.*
FDA Label Image

Container1 (Container1)

Container1 (Container1)
Label for Olanzapine Tablets USP 2.5 mg by Dr. Reddy's Laboratories Ltd. The label indicates a film-coated tablet dosage form, 30 tablets per container, for oral use. It includes dispensing instructions for pharmacists to provide a medication guide, storage conditions, and a barcode. The label features a combination of blue and orange text on a white background with the Dr. Reddy's logo.*
FDA Label Image

Srtucture (Structure)

Srtucture (Structure)
Chemical structure of olanzapine showing its molecular framework with nitrogen, sulfur, and methyl groups. The diagram depicts the connected atoms and rings characteristic of the olanzapine molecule.*

* 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.