Famotidine Tablet, Film Coated
Product Images NDC 58602-859

2 FDA label images from Aurohealth Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 58602-859). 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.

Product Images & Figures Index

FDA Label Image

Package Label-principal Display Panel -20 mg (50 Tablets, Container Label) (Famotidine 20mg Fig1)

Package Label-principal Display Panel -20 mg (50 Tablets, Container Label) (Famotidine 20mg Fig1)
The label for Famotidine tablets USP 20 mg by Aurohealth LLC displays the product as an acid reducer with 85 tablets per bottle. The label highlights it as a heartburn and acid indigestion relief in a single tablet dose. Warnings and usage instructions are printed in small text alongside product identification and manufacturer details.*
FDA Label Image

Package Label-principal Display Panel -20 mg (200 Tablets, Container Carton Label) (Famotidine 20mg Fig2)

Package Label-principal Display Panel -20 mg (200 Tablets, Container Carton Label) (Famotidine 20mg Fig2)
The image shows the unfolded carton packaging for Famotidine 20 mg film-coated tablets, an acid reducer by Aurohealth LLC. The package indicates it contains 85 tablets. The design features yellow and blue colors with text highlighting the product's use for acid reflux relief. The label includes Drug Facts, directions, warnings, inactive ingredients, and contact information for questions.*

* 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.