Clonazepam Tablet
Product Images NDC 80425-0125

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Clonazepam (NDC 80425-0125). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Pharmacy Of Tennessee, 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

Clonazepam 0.5mg Tab Qty 30 Ndc 80425 0125

Label for Clonazepam 0.5 mg oral tablets, packaged by Advanced Rx Pharmacy of Tennessee, LLC. The label includes a 30-count package size, lot number, expiration date, storage instructions, and a note that it is a prescription drug. It references generic equivalence to Klonopin.*

FDA Label Image

Clonazepam 0.5mg Tab Qty 60 Ndc 80425 0125

Label for Clonazepam 0.5 mg tablets, supplied by Advanced Rx Pharmacy of Tennessee, LLC in Nashville, TN. The label includes text indicating the product is comparable to Klonopin, with NDC code 80425-0125-02 and batch lot information. Storage instructions specify keeping the product at 20-25°C (68°-77°F).*

FDA Label Image

Clonazepam 0.5mg Tab Qty 90 Ndc 80425 0125

Clonazepam 0.5 mg tablet label from Advanced Rx Pharmacy of Tennessee, LLC, Nashville, TN. The label includes the product name, strength, tablet form, a comparison to Klonopin, NDC number 80425-0125-03, lot number, expiration date, manufacturer Accord Healthcare, and storage instructions. Packaging includes a barcode and federal caution information.*

FDA Label Image

Image

Chemical structure of the active ingredient clonazepam, showing its fused benzodiazepine ring system with a nitro group and a chlorophenyl substituent.*

* 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.