Olanzapine Tablet, Film Coated
Product Images NDC 68084-525

10 FDA label images from American Health Packaging · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Olanzapine (NDC 68084-525). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

10 mg Blister

10 mg Blister
Packaging label for Olanzapine 10 mg film-coated tablets by American Health Packaging. The label includes the drug name, dosage strength, formulation as a tablet USP, lot number 123456, and expiration date 04/17. Barcodes and labeler information are also present on the label sheet containing multiple identical labels.*
FDA Label Image

10 mg Carton

10 mg Carton
Packaging label for Olanzapine Tablets, USP 10 mg, film-coated oral tablets by American Health Packaging. The label indicates a package size of 100 tablets (10 x 10) with National Drug Code (NDC) 68084-740-01. Additional information includes storage instructions, a pharmacist dispensing note, and a drug source statement citing Dr. Reddy's Laboratories Limited.*
FDA Label Image

2 5 mg Blister

2 5 mg Blister
Olanzapine 2.5 mg oral film-coated tablet label from American Health Packaging. The label shows the product name, strength (2.5 mg), dosage form (tablet, USP), lot number (123456), and expiration date (04/17). The layout includes multiple identical label sections with barcodes for packaging.*
FDA Label Image

2 5 mg Carton

2 5 mg Carton
Olanzapine 2.5 mg film-coated tablets label showing 100 tablets (10 x 10) by American Health Packaging. The label includes NDC number 68084-525-01, dispensing instructions for pharmacists, storage conditions, and safety warnings to keep out of reach of children and not use if the blister is torn or broken.*
FDA Label Image

5 mg Blister

5 mg Blister
Sheet of multiple identical labels for Olanzapine 5 mg film-coated tablets by American Health Packaging. Each label includes the product name, strength (5 mg), dosage form (tablet, USP), placeholders for lot number and expiry date, a barcode, and manufacturer information.*
FDA Label Image

5 mg Carton

5 mg Carton
Olanzapine Tablets, USP 5 mg film-coated tablets packaging label. The label indicates 100 tablets (10 x 10) in the package. It includes storage instructions, pharmacist dispensing guidelines, and manufacturer information identifying American Health Packaging as the distributor and Dr. Reddy's Laboratories Limited as the original manufacturer. The label also displays the NDC number 68084-723-01 and a barcode.*
FDA Label Image

Ahp52501

Ahp52501
Olanzapine 2.5 mg film-coated oval tablet with imprints 'R 2.5' on one side and '0163' on the other side. The tablet is white and intended for oral administration. Manufactured by American Health Packaging.*
FDA Label Image

Ahp72301

Ahp72301
Olanzapine 5 mg film-coated tablet, oval and white, marked with 'R 5' on one side and '0164' on the other. Manufactured by American Health Packaging for oral administration.*
FDA Label Image

Ahp74001

Ahp74001
Olanzapine 10 mg film-coated tablet, white, oval-shaped with imprint 'R 10' on one side and '0166' on the other. This oral solid dosage form is manufactured by American Health Packaging.*
FDA Label Image

Structure

Structure
Chemical structure of Olanzapine, showing its ring system with sulfur and nitrogen atoms, including a methyl group attached to the piperazine ring and a methyl group on the thiophene ring.*

* 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.