Famotidine Tablet, Film Coated
Product Images NDC 54257-180

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 54257-180). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Magno-humphries, 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

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

Package Label-principal Display Panel -10 mg (90 Tablets, Container Label) (Famotidine Fig1)
Drug Facts panel for Famotidine 10 mg film-coated tablets by Magno-Humphries Labs. Active ingredient is famotidine USP, an acid reducer. The panel includes uses, warnings including allergy alert and when to stop use, directions for adults and children 12 years and older, inactive ingredients, and tips for managing heartburn. It also provides contact information and storage instructions, noting the product is manufactured and distributed by Johnson & Johnson and Merck Consumer Pharmaceuticals, made in India.*

* 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.