Cyclobenzaprine Hydrochloride Tablet, Film Coated
Product Images NDC 85534-0005

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Cyclobenzaprine Hydrochloride (NDC 85534-0005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hawaii Repack, 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

Image (Cyclobenzaprine HCl Tabs Structure)

Chemical structure of cyclobenzaprine hydrochloride, showing the molecular arrangement with fused rings and a side chain including nitrogen and hydrochloride components.*

FDA Label Image

10 (Label 10mg)

Labels for Cyclobenzaprine HCl Tablets USP 10 mg film-coated oral tablets, distributed by Hawaii Repack, Inc., showing package quantities of 30, 60, 90, and 120 tablets. Each label includes NDC codes, distributor information (Advagen Pharma Ltd.), and storage instructions. Tablets are described as orange-yellow, round, film-coated, and debossed.*

FDA Label Image

5 (Label 5mg)

Four labels for Cyclobenzaprine HCl Tablets USP 5 mg, distributed by Hawaii RePack, located in Honolulu, HI. Each label shows different NDC codes and quantities (30, 60, 90, 120 tablets) with information on distribution by Advagen Pharma Limited. The tablets are described as film-coated and debossed with a source NDC, including cautionary and storage instructions.*

FDA Label Image

7.5 (Label 7 5mg)

Four packaging labels for Cyclobenzaprine HCl Tablets USP 7.5 mg film-coated tablets. Distributed by Hawaii RePACK, each label lists different NDC codes and quantities: 30, 60, 90, and 120 tablets. Labels include distributor and source details, storage instructions, caution statements, and QR codes.*

* 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.