Famotidine Tablet, Film Coated
Product Images NDC 58602-829

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 58602-829). 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 -20 mg (100 Tablets, Container Label) (Famotidine 20mg Fig1)

PrimaryHealth Famotidine 20 mg Tablets USP maximum strength acid reducer packaging label. This oral film-coated tablet package contains 85 tablets, labeled as a heartburn and acid indigestion preventer and reliever. The label includes warnings, usage directions, storage instructions, lot, and expiration date fields. Manufactured for Aurohealth LLC.*

FDA Label Image

Package Label-principal Display Panel -20 mg (100 Tablets, Container Carton Label) (Famotidine 20mg Fig2)

Box label for Famotidine Tablets USP 20 mg by Aurohealth LLC under the PrimaryHealth brand. It is an over-the-counter acid reducer, maximum strength, with 85 film-coated tablets per container. The label highlights use for heartburn due to acid indigestion and includes Drug Facts, warnings, directions, and inactive ingredients. The product NDC is 58602-829-50.*

* 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.