Mirtazapine Tablet, Film Coated
Product Images NDC 63187-471

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Mirtazapine (NDC 63187-471). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

63187-206-60 (15mg30tablets)

63187-206-60 (15mg30tablets)
This is a description of a medication called Mirtazapine which is available in 15mg tablets. This product comes in a packaged bottle with 30 tablets from the manufacturer Apotex Inc. in Canada. The tablets are oval-shaped, scored and film-coated with the imprint of "APO" on one side and "M | 15" on the other side. The medication guide should be dispensed to each patient separately. The product should be stored between 20°-25°C (68°-77°F) and kept out of the reach of children. This product has been relabeled by Proficient Rx.*
FDA Label Image

63187-471-30 (45mg30tablets)

63187-471-30 (45mg30tablets)
This is a medication information for Mirtazapine 45mg tablets, distributed by ProficientRx. The tablets are white to off-white, oval-shaped, unscored, and film-coated. Each tablet is imprinted with "APO" on one side and "MI-45" on the other side. The medication should be kept at 20°-25°C (68°-77°F) and stored out of reach of children. The lot number is 00000, and the expiration date is 00/00/00. The package contains #30 tablets and a medication guide to be given to each patient. The NDC number is 63187-471-30. The tablets were manufactured by Apotex Inc. in Toronto, Ontario, Canada.*
FDA Label Image

Structure (Structure)

* 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.