Cyclobenzaprine Hcl Tablet, Film Coated
Product Images NDC 72189-680

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 Cyclobenzaprine Hcl (NDC 72189-680). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct_rx, 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

72189-680-30 (72189 680 30)

72189-680-30 (72189 680 30)
Cyclobenzaprine HCL 10 mg film-coated tablets in a 30 count pack by Direct Rx. The label states the product is generic for Flexeril and each film-coated tablet contains 10 mg of cyclobenzaprine hydrochloride USP. The label includes lot number, packaging details, and manufacturer information for SOLA Pharmaceuticals.*
FDA Label Image

72189-680-60 (72189 680 60)

72189-680-60 (72189 680 60)
Cyclobenzaprine HCL 10 mg film-coated tablets, packaged in a bottle containing 60 tablets. The label indicates the product is generic for Flexeril and contains cyclobenzaprine hydrochloride USP 10 mg per tablet. It is distributed by Direct_Rx and includes lot and expiration details for sample use.*
FDA Label Image

72189-680-90 (72189 680 90)

72189-680-90 (72189 680 90)
Label for Cyclobenzaprine HCL 10 mg film-coated tablets, in a 90 count package. The label notes Cyclobenzaprine hydrochloride USP 10 mg as the active ingredient, marketed as the generic equivalent of Flexeril. The product is labeled and distributed by Direct Rx with NDC 72189-680-90, lot number and expiration date also visible.*

* 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.