Famotidine Tablet, Film Coated
Product Images NDC 72657-132

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 72657-132). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Glenmark Therapeutics Inc., Usa, 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

Carton10mg90 (Carton10mg90)

Famotidine Tablets USP 10 mg film-coated tablets packaging label from Glenmark Therapeutics Inc., USA. The label highlights acid reducer properties, original strength, and a package count of 90 tablets. It includes detailed Drug Facts, usage instructions, warnings, inactive ingredients, and distributor information. The label also advises on managing heartburn and safe usage precautions.*

FDA Label Image

Carton20mg85 (Carton20mg85)

Famotidine Tablets, USP 20 mg film-coated oral tablets in a package containing 85 tablets, labeled as maximum strength acid reducer by Glenmark Therapeutics Inc., USA. The front panel highlights relief from heartburn due to acid indigestion and notes it contains the equivalent active ingredient in Pepcid AC. Drug Facts panels detail active ingredient, usage, warnings, directions, and additional product information.*

* 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.