Clonazepam Tablet
Product Images NDC 70518-4074

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Clonazepam (NDC 70518-4074). 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.

FDA Label Image

Remedy_label (Remedy Label)

Clonazepam 1 mg tablet label showing quantity of 30 tablets. The label includes the brand name ClonazePAM, classification C-IV, and is marked RX only. Manufacturer is Aurobindo, with repackaging by RemedyRepack Inc. The label also advises to keep out of reach of children and to see package insert for directions.*

FDA Label Image

Mm2 (Clonazepam 1mg 70518 4074 01)

Label for Clonazepam 1 mg tablet by RemedyRepack Inc. The label shows the product is a Schedule IV controlled substance (C-IV) and includes a quantity of 100 tablets per box. It states the drug is RX only and provides manufacturer information as Aurobindo, India. Directions refer to the package insert.*

FDA Label Image

Mm3 (Clonazepam 1mg 70518 4074 02)

Label for Clonazepam 1 mg tablet, a Schedule IV oral medication. The label shows the product name ClonazePAM and indicates a quantity of 1 tablet. The labeler is RemedyRepack Inc., with manufacturing attributed to Aurobindo in India. Includes caution statements, directions to see package insert, and storage temperature guidelines. The label includes a barcode and NDC 70518-4074-02.*

FDA Label Image

Chemical Structure (Clonazepam Str)

Chemical structure of clonazepam, showing its molecular framework with nitro, chlorine, and benzodiazepine ring features.*

* 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.