Epinephrine Injection, Solution, Concentrate
Product Images NDC 63323-696

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 Epinephrine (NDC 63323-696). 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

Figure (Epi04 0004 01)

Figure (Epi04 0004 01)
Chemical structure of epinephrine, showing the molecular arrangement relevant to its active ingredient composition.*
FDA Label Image

Figure (Epi04 0004 02)

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Epinephrine Injection, USP 1 mL Single-Dose Vial Label)

Package Label (PRINCIPAL DISPLAY – Epinephrine Injection, USP 1 mL Single-Dose Vial Label)
Label for Epinephrine Injection, USP 1 mg/mL by Fresenius Kabi USA, LLC. The product is a 1 mL single-dose vial concentrate for injection, with directions to dilute before intravenous and intraocular use. The label specifies intramuscular, intravenous, subcutaneous, and intraocular routes of administration.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – Epinephrine Injection, USP 1 mL Tray Label)

Package Label (PRINCIPAL DISPLAY – Epinephrine Injection, USP 1 mL Tray Label)
Label for Epinephrine Injection, USP 1 mg/mL by Fresenius Kabi USA, LLC. It includes usage instructions for dilution before intravenous and intraocular use, with recommended administration routes of intravenous infusion, intramuscular, subcutaneous, and intraocular. The label also states contents per mL and storage conditions, and indicates the package contains 25 single-dose 1 mL vials.*

* 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.