Mirtazapine Tablet, Film Coated
Product Images NDC 60687-584

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Mirtazapine (NDC 60687-584). 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

Ahp58421

Mirtazapine 7.5 mg film-coated tablet for oral use. The oblong white tablet is embossed with 'A' on one side and '11' on the other. Manufactured by American Health Packaging.*

FDA Label Image

7.5 mg Mirtazapine Tablets Carton (Carton)

Mirtazapine 7.5 mg film-coated tablets label by American Health Packaging. The label shows the product name, strength, dosage form, quantity of 30 tablets (3 x 10), and the NDC number 60687-584-21. It includes a barcode, pharmacist dispensing instructions, active ingredient information, storage conditions, safety warnings, distributor details, and Rx only designation.*

FDA Label Image

Chemical Structure (Structure)

Chemical structure diagram of mirtazapine, the active ingredient in this prescription drug. The structure shows multiple fused rings including nitrogen atoms, illustrating the molecular framework of mirtazapine.*

FDA Label Image

Image 01

Label sheet featuring multiple identical labels for Mirtazapine Tablet, USP 7.5 mg film-coated tablets. Each label includes the drug name, strength, placeholder lot number, and expiry date. The labeler American Health Packaging is indicated with location information for California, USA. Barcodes are present on each label.*

* 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.