Famotidine Tablet
Product Images NDC 68001-494

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 68001-494). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories, 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

Famotidine Tablets (Famotidine Tablets Bpl Carton Rev 03 21)

Famotidine Tablets (Famotidine Tablets Bpl Carton Rev 03 21)
Packaging label for Famotidine 10 mg tablets USP by BluePoint Laboratories. The label identifies the product as an acid reducer that prevents and relieves heartburn due to acid indigestion. It includes a barcode, directions for use, drug facts, warnings, storage instructions, and contact information. The label indicates the package contains 30 tablets and lists the manufacturer as Aurobindo Pharma Limited.*
FDA Label Image

Famotidine Tablets (Famotidine Tablets Bpl Label Rev 03 21)

Famotidine Tablets (Famotidine Tablets Bpl Label Rev 03 21)
Famotidine 10 mg tablets USP original strength packaging label by BluePoint Laboratories. This OTC oral acid reducer comes in a bottle of 30 tablets. The label includes warnings about allergies, usage directions, storage instructions, and contact information for the manufacturer. It states the product prevents and relieves heartburn and acid indigestion and emphasizes taking just one tablet. The label also displays the NDC 68001-494-04 and has detailed regulatory and safety information.*

* 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.