Famotidine Tablet, Film Coated
Product Images NDC 21130-033

View Photos of 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 21130-033). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Better Living Brands, 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 (25 Tablets, Container Label) (Famotidine 20mg Fig1)

Package Label-principal Display Panel -20 mg (25 Tablets, Container Label) (Famotidine 20mg Fig1)
Famotidine Tablets USP 20 mg film-coated tablets label from Better Living Brands, LLC. The label identifies the product as an acid controller and acid reducer for heartburn relief. The package contains 25 tablets. The label also includes warnings, usage instructions, and manufacturer information along with the NDC number 21130-033-53.*
FDA Label Image

Package Label-principal Display Panel -20 mg (25 Tablets, Container Carton Label) (Famotidine 20mg Fig2)

Package Label-principal Display Panel -20 mg (25 Tablets, Container Carton Label) (Famotidine 20mg Fig2)
Packaging label for Famotidine 20 mg film-coated tablets by Better Living Brands LLC, an over-the-counter acid reducer and acid controller. The label highlights maximum strength, acid control, and a count of 25 tablets. It includes branding by Signature Care, barcode, QR code for more information, and dosage claims related to heartburn relief from acid indigestion.*

* 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.