Chemical Structure (Famotidine 01)
Famotidine Tablet, Coated
Product Images NDC 69367-401
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 69367-401). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Westminster Pharmaceuticals, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
Principal Display Panel (20 mg Tablet Bottle Label)
This is a description of Famotidine USP 20 mg tablets, which are film-coated and intended for prescription use. The dosage and usage information should be referred to in the prescribing information. The tablets should be stored at a temperature between 15°C to 30°C (59°F to 86°F) and kept away from children. The manufacturer is listed as Contract Pharmacal Corp. with an address in Hauppauge, NY, USA. The packaging includes 1000 tablets and is distributed by Westminster Pharmaceuticals, LLC. The Pharmaceutical Review date is 08/2024, and the National Drug Code (NDC) is 69367-400-10.*
Principal Display Panel (40 mg Tablet Bottle Label)
This text is an evaluation of Famotidine tablets, USP, with 40 mg strength in a pack of 1000 tablets. It includes information on dosage, storage conditions, manufacturer details, and directions for dispensing. The medication is prescription only and should be kept out of reach of children. It is manufactured by Contract Pharmacal Corp and distributed by Westminster Pharmaceuticals, LLC. The revision date provided is 08/2024.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
