Famotidine Injection
Product Images NDC 67457-457

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 67457-457). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Institutional 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.

FDA Label Image

Image 01

Image 01
Packaging label for Famotidine Injection, USP 20 mg/2 mL (10 mg/mL) sterile intravenous injection single-dose vials. The label shows the product name, strength, dosage form, route, and sterile status. It is manufactured by Mylan Institutional LLC and comes in a pack of 25 x 2 mL vials. Storage instructions and inactive ingredients are also listed on the label.*
FDA Label Image

Image 02

Image 02
The packaging label for Famotidine Injection USP 40 mg/4 mL (10 mg/mL), supplied as a sterile intravenous injection by Mylan Institutional LLC. The carton is designed for 10 multi-dose vials of 4 mL each. The label includes storage instructions, active and inactive ingredients, and states use is for intravenous administration only after dilution. Manufactured for Mylan Institutional LLC, Rockford, IL.*
FDA Label Image

Image 03

Image 03
Label for Famotidine Injection, USP 200 mg/20 mL (10 mg/mL) sterile injection for intravenous use after dilution. The label shows packaging for 10 multi-dose vials of 20 mL each. Manufactured for Mylan Institutional LLC, with storage instructions and active ingredient details included.*
FDA Label Image

Image 04

Image 04
Chemical structure of famotidine, showing its molecular connectivity including the thiazole ring and sulfonamide groups.*

* 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.