Famotidine Tablet, Film Coated
Product Images NDC 64980-623

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 64980-623). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rising Pharma Holdings, Inc., 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

Image (3f43a0a4 1606 4d45 95c0 46b73e504010 01)

FDA Label Image

Image (3f43a0a4 1606 4d45 95c0 46b73e504010 02)

Image (3f43a0a4 1606 4d45 95c0 46b73e504010 02)
This text is not-readable.*
FDA Label Image

Image (3f43a0a4 1606 4d45 95c0 46b73e504010 03)

Image (3f43a0a4 1606 4d45 95c0 46b73e504010 03)
This is a description for Famotidine tablets, USP, containing 100 tablets with each film-coated tablet containing 40mg of Famotidine USP. The usual dosage information is available in the package insert. It should be stored at 20° to 25°C (68° to 77°F) with excursions permitted to 15° to 30°C (59° to 86°F). The tablets should be dispensed in a USP tight, light-resistant container. The tablets are manufactured by Graviti Pharmaceuticals Pvt. Ltd. in Telangana, India. The distribution is done by Rising Pharma Holdings, Inc. in East Brunswick, NJ 08816.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.