Epinephrine Injection
Product Images NDC 80830-1659

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 Epinephrine (NDC 80830-1659). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Private Limited, 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

1 (Epinephrine Injection Usp 1 mgml Single Dose Vial 1)

1 (Epinephrine Injection Usp 1 mgml Single Dose Vial 1)
Chemical structure of R-(-)-Epinephrine, depicting its molecular arrangement including hydroxyl groups and an amine group attached to a benzene ring.*
FDA Label Image

1 (Epinephrine Injection Usp 1 mgml Single Dose Vial 2)

1 (Epinephrine Injection Usp 1 mgml Single Dose Vial 2)
Label for Epinephrine Injection, USP 1 mg/mL by Amneal Pharmaceuticals Private Limited. It specifies use for intravenous infusion, intramuscular, and subcutaneous administration. The label indicates it is a 1 mL single-dose vial and includes storage instructions, NDC 80830-1659, barcode, and placeholder for batch coding and expiration date.*
FDA Label Image

2 (Epinephrine Injection Usp 1 mgml Single Dose Vial 3)

2 (Epinephrine Injection Usp 1 mgml Single Dose Vial 3)
Label panel for Epinephrine Injection, USP 1 mg/mL by Amneal Pharmaceuticals Private Limited. The label indicates it is for intravenous, intramuscular, and subcutaneous use, supplied in 25 single-dose vials of 1 mL each. It includes usage instructions, storage conditions to protect from light and freezing, and manufacturer details, with a barcode and batch coding area.*

* 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.