Diazepam Injection, Solution
Product Images NDC 0409-1273

4 FDA label images from Hospira, Inc. · 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 Diazepam (NDC 0409-1273). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, Inc., 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

Chemical Structure (Diazepam 01)

Chemical Structure (Diazepam 01)
Chemical structure of Diazepam, showing its molecular arrangement including a chlorine-substituted benzodiazepine core and molecular weight of 284.74.*
FDA Label Image

Logo (Diazepam 02)

FDA Label Image

Principal Display Panel (2 mL Cartridge Label)

Principal Display Panel (2 mL Cartridge Label)
Label for Diazepam Injection, USP 10 mg/2 mL (5 mg/mL) in a 2 mL single-dose Carpuject sterile cartridge with Luer Lock. Intended for intramuscular or intravenous use. Distributed by Hospira, Inc., Lake Forest, IL. Includes dosing scale, lot, expiry fields, and product NDC 0409-1273-03.*
FDA Label Image

Principal Display Panel (2 mL Cartridge Carton)

Principal Display Panel (2 mL Cartridge Carton)
Packaging label for Diazepam Injection, USP 10 mg/2 mL (5 mg/mL) sterile cartridge units with Luer Lock, single-dose 2 mL Carpulectâ„¢ by Hospira, Inc. It includes usage instructions for intramuscular or intravenous use, storage conditions, and warnings. The label indicates the product is for Rx only and distributed by Hospira, Inc., Lake Forest, IL, USA.*

* 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.