Zyprexa
Product Images NDC 21695-142

3 FDA label images from Rebel Distributors Corp · 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 Zyprexa (NDC 21695-142). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Chemical Structure (A3c9ea17 3793 494a 8b32 44e48f9f4503 01)

Chemical Structure (A3c9ea17 3793 494a 8b32 44e48f9f4503 01)
Chemical structure of the active ingredient in Zyprexa, showing a complex bicyclic ring system with nitrogen and sulfur atoms, including methyl functional groups attached to the molecule.*
FDA Label Image

Zyprexa 5mg (A3c9ea17 3793 494a 8b32 44e48f9f4503 02)

Zyprexa 5mg (A3c9ea17 3793 494a 8b32 44e48f9f4503 02)
Zyprexa 5 mg tablet bottle label showing quantity of 30 tablets. The label includes the active ingredient Olanzapine 5 mg per tablet, lot and expiration date fields, and states the product is for prescription use only. Distributed by Physician Partners, Thousand Oaks, CA. Storage instructions specify controlled room temperature between 15 to 30 °C (59 to 86 °F).*
FDA Label Image

Zyprexa 20mg (A3c9ea17 3793 494a 8b32 44e48f9f4503 03)

Zyprexa 20mg (A3c9ea17 3793 494a 8b32 44e48f9f4503 03)
Zyprexa 20mg tablets packaging label from Physician Partner, distributed by Rebel Distributors Corp. The label shows NDC 21695-144-30, containing 30 tablets per bottle. Each pink, elliptical, film-coated tablet contains 20mg of olanzapine. The label includes storage instructions and prescription-only designation.*

* 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.