Alprazolam Tablet
Product Images NDC 63187-971

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Alprazolam (NDC 63187-971). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Chemical Structure (Alprazolam 01)

Chemical Structure (Alprazolam 01)
Chemical structure of alprazolam, showing its fused benzodiazepine and triazole rings with chlorine substitution.*
FDA Label Image

Chemical Structure (Alprazolam 02)

Chemical Structure (Alprazolam 02)
An illustration showing the segmentation of an Alprazolam 2 mg oral tablet into different dose portions. It depicts a complete 2 mg tablet, then a tablet divided into two 1 mg segments, and finally a tablet segmented into four 0.5 mg parts for dosing flexibility.*
FDA Label Image

Logo 1 (Alprazolam 03)

Logo 1 (Alprazolam 03)
Label from a Greenstone brand product distributed by Greenstone LLC, Peapack, NJ 07977. The label includes the Greenstone logo and company name with distribution information. No specific drug name, dosage, or form is visible in this image.*
FDA Label Image

63187-971-30 (Alprazolam 07)

63187-971-30 (Alprazolam 07)
Alprazolam 2 mg tablets label from Proficient Rx LP. The label displays the product name, strength (2 mg), dosage form (tablets), quantity (#30), and indicates this is a Schedule IV controlled substance for prescription use only (RX Only). It includes storage instructions and packaging information from Proficient Rx LP in Thousand Oaks, CA.*

* 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.