Olanzapine Tablet, Film Coated
Product Images NDC 33342-072

13 FDA label images from Macleods Pharmaceuticals Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Olanzapine (NDC 33342-072). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Macleods Pharmaceuticals Limited, 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

138 (Olanzapine Tab Str)

138 (Olanzapine Tab Str)
Chemical structure of olanzapine, an antipsychotic medication. The diagram shows the molecular arrangement including nitrogen, sulfur atoms, and methyl groups characteristic of olanzapine's tetracyclic compound structure.*
FDA Label Image

123 (Olanzapine Tab 20 30s)

123 (Olanzapine Tab 20 30s)
Label for Olanzapine Tablets USP 20 mg film-coated tablets by Macleods Pharmaceuticals Limited. The label shows the product name, strength, quantity of 30 tablets, and storage instructions. It includes a pharmacist advisory about dispensing the Medication Guide and manufacturer information for Macleods Pharma USA and Macleods Pharmaceuticals Ltd in India.*
FDA Label Image

234 (Olanzapine Tab 15 30s)

234 (Olanzapine Tab 15 30s)
Label for Olanzapine Tablets USP 15 mg film coated tablets, oral dosage form. The package contains 30 tablets. The label references a pharmacist's instruction to dispense the accompanying medication guide. The product is manufactured for Macleods Pharma USA and by Macleods Pharmaceuticals Ltd in India. Storage instructions and usual dosage advisory are partially visible.*
FDA Label Image

555 (Olanzapine Tab 10 30s)

555 (Olanzapine Tab 10 30s)
Label for Olanzapine Tablets USP 10 mg, film-coated oral tablets. The label shows it is manufactured by Macleods Pharmaceuticals Limited, with the labeler as Macleods Pharma USA, Inc. The package contains 30 tablets. The label includes storage instructions and a note to dispense the accompanying Medication Guide. NDC 33342-070-07 is visible.*
FDA Label Image

678 (Olanzapine Tab 7 5 30s)

678 (Olanzapine Tab 7 5 30s)
Label for Olanzapine Tablets USP 7.5 mg, film-coated oral tablets, presented in a package containing 30 tablets. The label indicates the manufacturer as Macleods Pharmaceuticals Ltd., India, and the product is marketed by Macleods Pharma USA, Inc., New Jersey. Storage instructions and a barcode are also visible.*
FDA Label Image

888 (Olanzapine Tab 5 30s)

888 (Olanzapine Tab 5 30s)
Label for Olanzapine Tablets USP 5 mg, film-coated oral tablets, containing 30 tablets per bottle. Manufactured by Macleods Pharmaceuticals Ltd, India, and Macleods Pharma USA, Inc. The label includes storage instructions, dosage strength, National Drug Code (NDC 33342-068-07), and pharmacist dispensing instructions for accompanying medication guide.*
FDA Label Image

987 (Olanzapine Tab 2 5 30s)

987 (Olanzapine Tab 2 5 30s)
Label for Olanzapine Tablets USP 2.5 mg, film coated oral tablets, supplied in a container of 30 tablets. The label is from Macleods Pharmaceuticals Limited, manufactured for Macleods Pharma USA, Inc. It includes storage instructions, barcode, and a pharmacist dispensing notice. The product is prescription only.*
FDA Label Image

543 (Olanzapine Tab 20 10x10s)

543 (Olanzapine Tab 20 10x10s)
Packaging label for Olanzapine Tablets USP 20 mg, film-coated oral tablets. The label shows the product name, strength, and quantity of 100 tablets (10 x 10 unit dose blisters). It is distributed by Macleods Pharma USA, Inc. and manufactured by Macleods Pharmaceuticals Ltd. The label includes storage instructions and a note indicating the unit-dose package is not child resistant.*
FDA Label Image

444 (Olanzapine Tab 15 10x10s)

444 (Olanzapine Tab 15 10x10s)
Packaging label for Olanzapine Tablets, USP 15 mg film-coated tablets by Macleods Pharmaceuticals Limited. The package contains 100 tablets (10 x 10 unit dose blisters) manufactured for Macleods Pharma USA, Inc. The label includes storage instructions and a barcode.*
FDA Label Image

658 (Olanzapine Tab 10 10x10s)

658 (Olanzapine Tab 10 10x10s)
Olanzapine Tablets USP 10 mg film-coated oral tablets packaging label by Macleods Pharmaceuticals Limited. The label includes the product name, strength, NDC number 33342-070-12, manufacturer information, batch and expiration date fields, barcode, and storage instructions. The package contains 100 tablets in 10x10 unit dose blisters.*
FDA Label Image

688 (Olanzapine Tab 7 5 10x10s)

688 (Olanzapine Tab 7 5 10x10s)
Label for Olanzapine Tablets USP 7.5 mg film-coated tablets by Macleods Pharmaceuticals Limited. The package contains 100 tablets in 10 unit dose blister packs. The label includes storage instructions and manufacturer details for Macleods Pharma USA and Macleods Pharmaceuticals Ltd, India.*
FDA Label Image

777 (Olanzapine Tab 5 10x10s)

777 (Olanzapine Tab 5 10x10s)
Olanzapine Tablets USP 5 mg film-coated oral tablets packaging label from Macleods Pharmaceuticals Limited. The label includes the product name, strength, NDC 33342-068-12, quantity of 100 tablets in 10 unit dose blisters, storage instructions, and manufacturer information including Macleods Pharma USA and Macleods Pharmaceuticals Ltd. in India.*
FDA Label Image

800 (Olanzapine Tab 2 5 10x10s)

800 (Olanzapine Tab 2 5 10x10s)
Label for Olanzapine Tablets, USP 2.5 mg by Macleods Pharmaceuticals Limited. The label includes dosage strength 2.5 mg and states the packaging contains 100 tablets in 10 x 10 unit dose blisters. Manufacturer details mention Macleods Pharma USA, Inc. and manufacturing in India. Storage instructions and a note on child resistance are included.*

* 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.