Famotidine Tablet
Product Images NDC 61442-122

3 FDA label images from Carlsbad Technology, Inc · 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 61442-122). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Carlsbad Technology, 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

Structural Formula (Fam00 0002 01)

Structural Formula (Fam00 0002 01)
Chemical structure of famotidine, depicted as a molecular diagram showing its atoms and bonds, consistent with its role as the active ingredient in the drug Famotidine.*
FDA Label Image

Principal Display Panel – Bottle Label (Fam00 0002 04)

Principal Display Panel – Bottle Label (Fam00 0002 04)
Label for Famotidine 20 mg oral tablets by Carlsbad Technology, Inc. The label states 'Rx Only' and indicates a quantity of 100 tablets. It includes storage instructions for controlled room temperature and mentions dispensing in a tight container. A barcode and NDC number 61442-121 are visible.*
FDA Label Image

Principal Display Panel – Bottle Label (Fam00 0002 05)

Principal Display Panel – Bottle Label (Fam00 0002 05)
Famotidine 40 mg tablets label from Carlsbad Technology, Inc. The label states each tablet contains 40 mg of famotidine, with 100 tablets in the container. It indicates the dosage form as tablets oral and provides storage instructions at 20° to 25°C (68° to 77°F). The label includes the NDC code 61442-122-01 and notes the product is Rx only.*

* 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.