Famotidine Tablet, Film Coated
Product Images NDC 80425-0329

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 80425-0329). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Pharmacy Of Tennessee, 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

Description (Description)

Chemical structure of famotidine, the active ingredient in the product. The diagram shows the molecular arrangement including nitrogen, sulfur, and oxygen atoms in the famotidine molecule.*

FDA Label Image

Label 1 (Famotidine 20mg 80425 0329 01)

Famotidine 20 mg tablet film coated prescription drug label from Advanced Rx Pharmacy of Tennessee, LLC. The label indicates storage instructions at 20-25°C (68-77°F) and references a comparison to Pepcid. It includes a lot number, expiration date of 3/31/2024, and pharmacy details with serial number.*

FDA Label Image

Label 2 (Famotidine 20mg 80425 0329 02)

Famotidine 20 mg tablet film coated box label from Advanced Rx Pharmacy of Tennessee, LLC. Label states product NDC 80425-0329, lot and expiration date 3/31/2024. It includes a storage temperature range and a comparison to PEPCID with source NDC 31722-0017-01.*

FDA Label Image

Label 3 (Famotidine 20mg 80425 0329 03)

Famotidine 20 mg tablet film coated packaging label from Advanced Rx Pharmacy of Tennessee, LLC, Nashville, TN. Includes storage instructions at 20-25°C, barcode, and comparison to Pepcid. The label shows a lot number and expiration date of 3/31/2024, with the product NDC 80425-0329.*

FDA Label Image

Logo (Logo)

* 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.