Famotidine Injection, Solution
Product Images NDC 63323-739

4 FDA label images from Fresenius Kabi Usa, Llc · 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 63323-739). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

Fam03 0003 01

Fam03 0003 01
Chemical structure of famotidine showing the arrangement of carbon, hydrogen, nitrogen, oxygen, and sulfur atoms in the molecule. The image includes the molecular formula C8H15N7O2S3 and the molecular weight 337.45.*
FDA Label Image

Fam03 0003 02

Fam03 0003 02
Famotidine 10 mg/mL injection, solution in an intravenous dosage form, labeled by Fresenius Kabi USA, LLC. The label shows the Fresenius Kabi logo with location Lake Zurich, IL 60047, without further dosage or packaging information visible.*
FDA Label Image

Fam03 0003 03

Fam03 0003 03
Label for Famotidine Injection, USP, 20 mg per 2 mL (10 mg per mL) single-dose vial. The intravenous solution is labeled as Rx only. The label includes the NDC 63323-739-11 and is manufactured by Fresenius Kabi USA, LLC, located in Lake Zurich, IL. Instructions specify discarding unused portions.*
FDA Label Image

Fam03 0003 04

Fam03 0003 04
Label for Famotidine Injection, USP 20 mg per 2 mL (10 mg per mL) single dose vials, 25 vials of 2 mL each. The intravenous injection solution is labeled for use under the Fresenius Kabi USA, LLC labeler, with storage instructions and inactive ingredients listed. The product is for Rx use only and not for use with natural rubber latex closures.*

* 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.