Diazepam Injection, Solution
Product Images NDC 0409-3213

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 Diazepam (NDC 0409-3213). 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 with a molecular weight of 284.74, showing chlorine, nitrogen, carbon, and oxygen atoms arranged in the characteristic benzodiazepine ring system.*
FDA Label Image

Logo (Diazepam 02)

FDA Label Image

Principal Display Panel (10 mL Vial Label)

Principal Display Panel (10 mL Vial Label)
Label for Diazepam Injection, USP 5 mg/mL by Hospira, Inc. The vial contains 10 mL multiple-dose with a total of 50 mg Diazepam. The label includes concentration details, storage instructions, and usage warnings, stating it is for intravenous or intramuscular use only. The label also notes the solution may appear colorless to light yellow and includes preservative and excipient information.*
FDA Label Image

Principal Display Panel (10 mL Vial Box)

Principal Display Panel (10 mL Vial Box)
Diazepam Injection, USP 5 mg/mL (50 mg/10 mL) multiple dose vial packaging label. The label indicates the product is sterile, nonpyrogenic, for intravenous or intramuscular use, and includes protective storage instructions. Manufactured by Hospira, Inc., with NDC 0409-3213-12. The packaging details 10 mL vial size and states the solution may appear colorless to light yellow.*

* 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.