Chlorzoxazone Tablet
Product Images NDC 85766-282

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Chlorzoxazone (NDC 85766-282). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sportpharm Llc, 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

Str (Chlorzoxazone Str)

Chemical structure of chlorzoxazone, showing a benzene ring with a chlorine atom attached, connected to a heterocyclic ring containing oxygen and nitrogen atoms.*

FDA Label Image

375 (Label 375mg)

Labels for Chlorzoxazone Tablets USP 375 mg oral tablets repackaged or relabeled for Sportpharm LLC. Each label displays the drug name, strength (375 mg), NDC code, quantity (ranging from 10 to 100), distributor Aurobindo Pharma USA, Inc., and a description of the tablets as white to off-white capsule shaped and debossed N 375. The labels include barcodes, QR codes, lot and expiration fields, drug status as RX, and storage instructions.*

FDA Label Image

500 (Label 500mg)

Multiple labels for Chlorzoxazone Tablets, USP 500 mg, repackaged by Sportpharm LLC. Each label includes the NDC, quantity (ranging from 10 to 100 tablets), distributor info (Aurobindo Pharma USA, Inc.), a barcode, and standard caution and storage instructions. Batch and expiration fields are blank. The labels are for oral tablets in various package sizes.*

FDA Label Image

750 (Label 750mg)

Multiple repackaged labels for Chlorzoxazone Tablets, USP 750 mg by Sportpharm LLC. Each label shows varying package quantities (10, 14, 20, 28, 30, 60, 90, 100 tablets) with consistent details including NDC numbers, distributed by Aurobindo Pharma USA, Inc., and warning statements.*

* 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.