Famotidine Tablet, Film Coated
Product Images NDC 58602-705

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 58602-705). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurohealth Llc, 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

Package Label-principal Display Panel -10 mg (90 Tablets Container Label) (Famotidine Fig1)

The packaging label for Famotidine Tablets USP 10 mg by Aurohealth LLC displays the brand name 'Famotidine' with active strength 10 mg as film-coated tablets. It is labeled as an acid reducer to prevent and relieve heartburn and acid indigestion. The package contains 90 tablets. Additional text includes a warning section and labeling format information.*

FDA Label Image

Famotidine-fig2.jpg (Famotidine Fig2)

The packaging label for Famotidine Tablets USP 10 mg by Aurohealth LLC displays 90 film-coated oral tablets. The label highlights it as an acid reducer, intended to prevent and relieve heartburn due to acid indigestion. The front panel uses blue and red colors, with essential drug facts and directions detailed on side panels. The label also includes barcode, lot, and expiration placeholders.*

FDA Label Image

Famotidine-fig3.jpg (Famotidine Fig3)

Packaging label for Famotidine Tablets USP 10 mg, original strength, film-coated oral tablets. The label states it is an acid reducer with a package size of 30 tablets. Labeler is Aurohealth LLC. The front panel highlights use for relief and prevention of heartburn due to acid indigestion, and includes directions and drug facts on the back, detailing active ingredient, warnings, and inactive ingredients.*

* 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.