Diazepam Tablet
Product Images NDC 0172-3927

4 FDA label images from Teva Pharmaceuticals Usa, 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 0172-3927). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Pharmaceuticals Usa, 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.

Product Images & Figures Index

FDA Label Image

Image 1

Image 1
Chemical structure of Diazepam, depicting its molecular components including a chlorine-substituted benzene ring, a diazepine ring, and a methyl group attached to a nitrogen atom.*
FDA Label Image

Image 2

Image 2
Diazepam Tablets, USP 2 mg oral tablets label from Teva Pharmaceuticals USA, Inc. The label shows the drug name, strength (2 mg), dosage form (tablet), quantity (100 tablets), and instructions for pharmacists to dispense the medication guide. The label also includes a control number, barcode, and tamper-evident warning.*
FDA Label Image

Image 3

Image 3
Diazepam Tablets, USP 5 mg oral tablets in a 100 tablet package by Teva Pharmaceuticals USA, Inc. The label includes dosing strength, US federal warning, and a note for pharmacists to dispense the Medication Guide. It displays the NDC code 0172-3926-60 and Teva logo.*
FDA Label Image

Image 4

Image 4
Diazepam Tablets USP 10 mg oral tablets label from Teva Pharmaceuticals USA, Inc. The label indicates a pack size of 100 tablets, includes a controlled substance schedule IV symbol, and includes a note for pharmacists to dispense the accompanying Medication Guide to each patient. Additional regulatory and manufacturing information is printed on the label.*

* 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.