Clonazepam Tablet
Product Images NDC 0093-3213

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Clonazepam (NDC 0093-3213). 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.

FDA Label Image

Chem Structure (Image 1)

Chemical structure of Clonazepam, showing its fused benzodiazepine core with nitro and chloro substituents on the aromatic rings, consistent with its molecular configuration as an active pharmaceutical ingredient.*

FDA Label Image

New 1mg (Image 2)

Label for Clonazepam Tablets USP 0.5 mg oral tablets by Teva Pharmaceuticals USA, Inc. The bottle contains 100 tablets. The label includes the NDC 0093-0832-01, a control number, and a warning to pharmacists to dispense the accompanying Medication Guide to each patient. It is marked as a Schedule IV controlled substance and for prescription use only.*

FDA Label Image

New 2mg (Image 3)

Clonazepam Tablets, USP oral tablets from Teva Pharmaceuticals USA, Inc., 1 mg strength. The label indicates this is a prescription medication with a package count of 100 tablets. The design includes dosage strength highlighted in red and a controlled substance schedule IV symbol.*

FDA Label Image

Image 4

Clonazepam Tablets, USP 2 mg oral tablets label from Teva Pharmaceuticals USA, Inc. The label includes the DEA Schedule IV marking and states Rx only. The package contains 100 tablets. Additional instructions for pharmacists and medication guide dispensing are visible. Serialization coding and barcode are also present.*

* 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.