Carbamazepine Tablet, Extended Release
Product Images NDC 27241-232

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Carbamazepine (NDC 27241-232). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ajanta Pharma Usa 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

100mg (Carbamazepine 100mg)

Label for Carbamazepine Extended-Release Tablets, USP 100 mg by Ajanta Pharma USA Inc. The label states the product contains 100 extended-release oral tablets. Includes storage instructions, child-resistant packaging notice, and pharmacist dispensing guidance. Barcode and NDC 27241-231-01 are visible. The label indicates the tablets must be swallowed whole.*

FDA Label Image

200mg (Carbamazepine 200mg)

Label for Carbamazepine Extended-Release Tablets, USP 200 mg, in a package of 100 tablets. The label states the tablets must be swallowed whole and not crushed or chewed. It includes storage instructions, child-resistant packaging note, and labeler Ajanta Pharma USA Inc., Bridgewater, NJ. The tablets are made in India.*

FDA Label Image

400mg (Carbamazepine 400mg)

Label for Carbamazepine Extended-Release Tablets, USP 400 mg oral tablets by Ajanta Pharma USA Inc. The label indicates 100 tablets per package and includes storage instructions, dosage form, and pharmacist dispensing guidance. It states the product is child-resistant and to protect from moisture.*

FDA Label Image

Structure (Carbamazepine Structure)

Chemical structure diagram of carbamazepine, showing its characteristic dibenzazepine core with an amide substituent (CONH2) on the nitrogen atom.*

* 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.