Diazepam Tablet
Product Images NDC 70518-1713

3 FDA label images from Remedyrepack Inc. · 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 Diazepam (NDC 70518-1713). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
The packaging label for Diazepam 5 mg oral tablets displays the brand name diazePAM, strength (5 mg), dosage form (tablet), and quantity (30 tablets). The label indicates it is a Schedule IV controlled substance (C-IV) and is repackaged by RemedyRepack Inc. The label also includes barcodes, a QR code, NDC number 70518-1713-00, manufacturer details (Teva Pharma, North Wales, PA), and usage warnings.*
FDA Label Image

Diazepam 5mg 70518 1713 01

Diazepam 5mg 70518 1713 01
Label for Diazepam 5 mg oral tablet, packaged in a quantity of 30 tablets. The label includes the REMEDYREPACK INC. logo and shows it is a Schedule IV controlled substance (C-IV). Manufacturer is listed as Teva Pharma, North Wales, PA. Additional labeling includes an NDC barcode, QR code, warnings to keep medication out of reach of children, usage directions referencing the package insert, and storage instructions.*
FDA Label Image

Image 1

Image 1
Chemical structure of Diazepam showing its molecular components including a chlorophenyl group, a diazepine ring, and a methylated nitrogen atom.*

* 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.