Alprazolam
Product Images NDC 21695-248

View Photos of 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 Alprazolam (NDC 21695-248). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp., 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

Package Label (248)

Package Label (248)
Alprazolam 0.5 mg tablets #15 label with the National Drug Code (NDC) 21695-248-15. The label indicates the product ID PA024815 and states the tablets are oval, peach, debossed with "GG 257" on one side and scored on the reverse. Manufactured by Sandoz Inc., Princeton, NJ, and packaged by Physician Partner, Thousand Oaks, CA. It includes storage instructions and a prescription only designation.*
FDA Label Image

Package Label (249)

Package Label (249)
Alprazolam 1 mg tablets packaging label by Rebel Distributors Corp, featuring a Physician Partner logo. The label indicates the product is a Schedule IV controlled substance, with each oval blue tablet debossed 'GG 258' and scored. It includes lot number, expiration date, product ID PA024945, and manufacturer information for Sandoz Inc., Princeton, NJ. Storage instructions specify controlled room temperature 15°-30°C (59°-86°F).*
FDA Label Image

Chemical Structure (Alprazolam 01)

Chemical Structure (Alprazolam 01)
Chemical structure of Alprazolam showing the molecular formula C17H13ClN4 and molecular weight 308.77. The structure includes a chlorinated benzene ring, nitrogen atoms in a triazole ring, and attached aromatic groups.*

* 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.