Clonazepam
Product Images NDC 67046-914

3 FDA label images from Contract Pharmacy Services-pa · 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 Clonazepam (NDC 67046-914). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Contract Pharmacy Services-pa, 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

Chemicalstructure.jpg (Chemicalstructure)

Chemicalstructure.jpg (Chemicalstructure)
Chemical structure of Clonazepam showing a benzodiazepine core with nitro and chloro substituents on the aromatic rings.*
FDA Label Image

Clonazepam Tablets Usp 0.5 mg Civ 500s Label (D6db2ac2 93f8 4d95 915a Ed5fa80a023a 02)

Clonazepam Tablets Usp 0.5 mg Civ 500s Label (D6db2ac2 93f8 4d95 915a Ed5fa80a023a 02)
Clonazepam 0.5 mg tablet packaged in a bottle of 30 tablets. The label includes dosage strength, pill ID (832 TEVA), lot number (26C171), and expiration date (04/30/15). It states the product is a controlled substance (Schedule IV) and packaged by Contract Pharmacy Services-PA, Warrington, PA. Storage instructions note 20-25°C (68-77°F).*
FDA Label Image

Clonazepam Tablets Usp 2 mg Civ 500s Label (D6db2ac2 93f8 4d95 915a Ed5fa80a023a 04)

Clonazepam Tablets Usp 2 mg Civ 500s Label (D6db2ac2 93f8 4d95 915a Ed5fa80a023a 04)
Clonazepam 2 mg tablets label showing a bottle or packaging for 30 tablets. The label includes the drug name, strength, quantity, Rx Only status, controlled substance classification (Schedule IV), lot number, pill ID, expiration date, manufacturer TEVA, and packaging by Contract Pharmacy Services-PA. Storage instructions and dosage caution 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.