Famotidine Tablet
Product Images NDC 50268-304

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 50268-304). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avpak, 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

Label 1 (Screen Shot 2014 10 07 At 9.39.30 Am)

Label 1 (Screen Shot 2014 10 07 At 9.39.30 Am)
Famotidine Tablets USP 20mg is a prescription medicine available in two variations. One variation contains 50 tablets, with each tablet containing 20mg of Famotidine. This variation comes in a unit dose of 6 tablets per pack and is identified by number N5026830515. The other variation also contains 50 tablets, with each containing 20mg of Famotidine. It comes in a unit dose of 5 tablets per pack and is identified only by the letter "i". There is additional text present, but it seems to be a mix of random letters, numbers, and symbols not forming coherent text.*
FDA Label Image

Label 2 (Screen Shot 2014 10 07 At 9.39.50 Am)

Label 2 (Screen Shot 2014 10 07 At 9.39.50 Am)
This is a description of Famotidine Tablets USP, 40mg strength. The tablets come in a package with 50 tablets (6x10) in unit doses. There is a prescription number, but no other information is provided. It is unclear what "Degres 2 el o" and "St oot o g, 27 05T 77 o 5" mean. The text ends with "P 3078" and "W e 510 owep".*
FDA Label Image

Structural Formula (Fam00 0002 01)

FDA Label Image

Cti 121 (Fam00 0002 02)

FDA Label Image

Cti 122 (Fam00 0002 03)

* 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.