Mirtazapine Tablet, Film Coated
Product Images NDC 0615-8268

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Mirtazapine (NDC 0615-8268). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ncs Healthcare Of Ky, Inc Dba Vangard Labs, 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

Mirtazpine Structure (Mirtazapine Tabs 8268 8269 Aurolife 1)

Chemical structure of the active ingredient mirtazapine, showing its molecular framework including a tetracyclic system with nitrogen atoms and a methyl group attached to a nitrogen.*

FDA Label Image

Principal Display Panel-mirtazapine 15mg Tab Bingo Label (Mirtazapine Tabs 8268 8269 Aurolife 2)

Mirtazapine Tablets USP 15 mg film-coated tablets packaging label showing lot number 8268 and quantity of 30 tablets. Manufactured by Aurolife for Aurobindo and packaged by Vangard Labs, Glasgow, KY 42141. The label includes multiple barcodes for individual tablets and storage instructions (20°-25°C). The label states 'Rx only' and 'FOR INSTITUTIONAL USE ONLY.'*

FDA Label Image

Principal Display Panel-mirtazapine 30mg Tab Bingo Label (Mirtazapine Tabs 8268 8269 Aurolife 3)

Mirtazapine Tabs USP 30 mg film-coated tablets label for prescription use. The label includes lot number 8269 and space for expiration date, with a quantity of 30 tablets. It is manufactured for Aurobindo and packaged by Vangard Labs in Glasgow, KY. The label includes instructions to store at 20°-25°C and to dispense in a tight, light-resistant container, indicating use for institutional dispensing.*

* 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.