Zolpidem Tartrate Tablet, Coated
Product Images NDC 63187-691

3 FDA label images from Proficient Rx Lp · 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 Zolpidem Tartrate (NDC 63187-691). 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 (2963ec25 A1f1 403a A539 Bce7b19d46d0 01)

Chemical Structure (2963ec25 A1f1 403a A539 Bce7b19d46d0 01)
Chemical structure of zolpidem tartrate showing its molecular arrangement with two main components, including the zolpidem molecule and tartrate moiety.*
FDA Label Image

63187-691-60 (2963ec25 A1f1 403a A539 Bce7b19d46d0 02)

63187-691-60 (2963ec25 A1f1 403a A539 Bce7b19d46d0 02)
Zolpidem Tartrate 5 mg coated tablets package label by Proficient Rx LP. Contains 60 tablets per bottle. The label indicates the product is a C-IV controlled substance, prescription only, with storage instructions and manufacturer information. Tablets are described as white, round, biconvex film-coated with ZLP debossed on one side and 5 on the other.*
FDA Label Image

63187-690-30 (2963ec25 A1f1 403a A539 Bce7b19d46d0 03)

63187-690-30 (2963ec25 A1f1 403a A539 Bce7b19d46d0 03)
Label for Zolpidem Tartrate 10 mg coated tablets, with 30 tablets per package. The label shows the ProficientRx logo, NDC 63187-690-30, and indicates it is a C-IV prescription drug. Tablets are described as yellow, round-shaped, biconvex, film-coated with debossed markings. Manufactured in Slovenia by Lek Pharmaceuticals d.d. and packaged by 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.