Carbamazepine Er Tablet, Extended Release
Product Images NDC 62135-928

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Carbamazepine Er (NDC 62135-928). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chartwell Rx, 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

"image Description" (Carbamazepine Er Tabs 100mg Bottle Label)

Carbamazepine Extended-Release Tablets USP 100 mg oral tablets packaging label from Chartwell RX, LLC. The label indicates 60 tablets per bottle with instructions to swallow whole and not crush or chew. NDC 62135-927 is displayed along with storage and dispensing information.*

FDA Label Image

"image Description" (Carbamazepine Er Tabs 200mg Bottle Label)

Label for Carbamazepine Extended-Release Tablets, USP 200 mg by Chartwell RX, LLC. The label states it contains 60 tablets, with directions that tablets must be swallowed whole, not crushed or chewed. Storage instructions and manufacturer details are included, along with a barcode and the text 'No Varnish' on the right edge.*

FDA Label Image

"image Description" (Carbamazepine Er Tabs 400mg Bottle Label)

Label for Carbamazepine Extended-Release Tablets USP 400 mg by Chartwell RX, LLC. The label indicates 60 tablets per bottle with NDC 62135-930-60. It includes directions to swallow tablets whole, storage instructions between 20° to 30°C, and warnings to keep out of reach of children. The label bears the Chartwell RX logo and barcode.*

FDA Label Image

"image Description" (Carbamazepine Er Tabs Structure)

Chemical structure diagram of carbamazepine showing its three-ring system with nitrogen and an amide group (CONH2) attached.*

* 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.