Famotidine
Product Images NDC 70860-753

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Famotidine (NDC 70860-753). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Athenex Pharmaceutical Division, 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

Fam05 0003 01

Chemical structure diagram of famotidine showing its molecular framework with nitrogen, sulfur, and oxygen atoms, consistent with the active ingredient famotidine from Athenex Pharmaceutical Division, LLC.*

FDA Label Image

Fam05 0003 02

Famotidine Injection, USP label from Athenex Pharmaceutical Division, LLC. The vial contains 20 mg per 2 mL (10 mg per mL) for intravenous use only. It is a 2 mL single-dose vial, sterile, nonpyrogenic, and preservative-free. The label includes storage instructions and manufacturing details, including Made in India and Athenex Schaumburg, IL address. A barcode and lot/expiration date fields are also visible.*

FDA Label Image

Fam05 0003 03

Label for Famotidine Injection, USP, 40 mg per 4 mL (10 mg per mL), in a 4 mL two-dose vial. The label indicates it is sterile, nonpyrogenic, and for intravenous use only after dilution. Manufactured for Athenex Pharmaceutical Division, LLC, Schaumburg, IL, and made in India.*

FDA Label Image

Fam05 0003 04

Famotidine Injection, USP 200 mg per 20 mL (10 mg per mL) multi-dose vial label from Athenex Pharmaceutical Division, LLC. The label specifies it is for preparation of intravenous solutions for intravenous use only after dilution, and includes storage instructions, sterile, nonpyrogenic statement, and a barcode.*

* 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.