Mirtazapine Tablet, Film Coated
Product Images NDC 0378-3545

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Mirtazapine (NDC 0378-3545). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Pharmaceuticals Inc., 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

Mirtazapine Stuctural Formula (Image 01)

Label for Mirtazapine 15 mg film-coated tablets, USP, manufactured by Mylan Pharmaceuticals Inc. The label includes dosage strength (15 mg), quantity (30 tablets), and instructions to dispense the medication guide. Storage and handling instructions note to keep the container tightly closed, store at controlled room temperature, and protect from light and moisture. The label features the Mylan logo and specifies the drug is for oral use and prescription only.*

FDA Label Image

Image 02

Mirtazapine 30 mg tablets, USP, film-coated oral tablets, manufactured by Mylan Pharmaceuticals Inc. The label includes the NDC 0378-3530-93, dosage strength, quantity of 30 tablets, and storage instructions. It also displays the Mylan logo and indicates prescription use only.*

FDA Label Image

Image 03

Label for Mirtazapine 45 mg film-coated tablets by Mylan Pharmaceuticals Inc., containing 30 tablets. The label shows the NDC number 0378-3545-93, directions for storage at 20° to 25°C, child-resistant packaging instructions, and a reminder to dispense the medication guide to patients. The label includes Mylan logos and the tablet imprint 'M 545'.*

FDA Label Image

Image 04

Chemical structure of mirtazapine, showing interconnected rings including a pyridine and a piperazine moiety with a methyl group attached to a nitrogen atom.*

* 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.