Diazepam Injection, Solution
Product Images NDC 69339-137

4 FDA label images from Natco Pharma 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 Diazepam (NDC 69339-137). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Natco Pharma 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

Molecular Structure Of Diazepam Injection (Diazepam 01)

FDA Label Image

Vial Label (Diazepam 02)

Vial Label (Diazepam 02)
Chemical structure of Diazepam showing its molecular formula with a chlorine-substituted benzene ring and a diazepine ring. The molecular weight is indicated as 284.74.*
FDA Label Image

10 Pack Carton Label (Diazepam 03)

10 Pack Carton Label (Diazepam 03)
Label for Diazepam Injection, USP 50 mg/10 mL (5 mg/mL) multiple-dose vial by Natco Pharma USA LLC. The label includes dosage information, storage instructions, and manufacturer details, specifying use for intravenous or intramuscular injection with protection from light. The NDC is 69339-137-01.*
FDA Label Image

5 Pack Carton Label (Diazepam 04)

5 Pack Carton Label (Diazepam 04)
Packaging label for Diazepam Injection, USP 5 mg/mL (50 mg/10 mL) in a 10 mL multi-dose vial. The label includes dosage form and strength, instructions for intravenous or intramuscular use, storage conditions, and manufacturer information for Natco Pharma USA LLC. The NDC number 69339-137-05 is displayed, along with a Barcode and the Rx only designation.*

* 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.