Famotidine Tablet, Film Coated
Product Images NDC 67296-2264

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 67296-2264). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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
FDA Label Image

Famotabstructure (Famotabstrucure)

Famotabstructure (Famotabstrucure)
Chemical structure of Famotidine, an active ingredient shown in the diagram with its distinct sulfur, nitrogen, oxygen, and hydrogen atoms arranged in molecular bonds.*
FDA Label Image

Famtab20mg100scontlabel (Famtab20mg100scontlabel)

Famtab20mg100scontlabel (Famtab20mg100scontlabel)
Famotidine 20 mg film-coated tablets label by Camber Pharmaceuticals, Inc. The label shows that the product is a USP prescription drug, with 100 tablets per container. Storage instructions and manufacturer details, including Annora Pharma Pvt. Ltd. in India, are printed alongside a barcode and contact information. The label includes a blank area for batch coding details.*
FDA Label Image

Famtab40mg100scontlabel (Famtab40mg100scontlabel)

Famtab40mg100scontlabel (Famtab40mg100scontlabel)
Famotidine Tablets, USP 40 mg film-coated tablets packaging label showing 100 tablets per container. The label includes storage instructions, a contact number, manufacturer details for Camber Pharmaceuticals, Inc., and Annora Pharma Pvt. Ltd. Location is New Jersey, USA and Telangana, India. The label features a barcode and a designated unvarnished area for batch coding details.*

* 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.