Carbamazepine Tablet, Extended Release
Product Images NDC 68382-556

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Carbamazepine (NDC 68382-556). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Pharmaceuticals (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

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Chemical structure of carbamazepine, showing a tricyclic compound with a central nitrogen atom and an attached amide group (CONH2).*

FDA Label Image

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Carbamazepine Extended-Release Tablets 100 mg label showing a film-coated, extended-release oral tablet. The label includes directions to dispense the Medication Guide separately, warnings about tablet swallowing, storage instructions, and manufacturer and distributor details. The label is from Zydus Pharmaceuticals (USA) Inc. and includes 100 tablets, Rx only.*

FDA Label Image

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Label for Carbamazepine Extended-Release Tablets 200 mg by Zydus Pharmaceuticals (USA) Inc. The film-coated extended-release tablets come in a package of 100 tablets for oral use. The label includes storage instructions, medication guide directions, barcode, and manufacturer/distributor information.*

FDA Label Image

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Label for Carbamazepine Extended-Release Tablets 400 mg from Zydus Pharmaceuticals (USA) Inc. The oral dosage form is film-coated extended-release tablets. The label indicates NDC 68382-557-01, package contains 100 tablets, and includes storage instructions, pharmacist dispensing guidance, and manufacturer information from Cadila Healthcare Ltd., India, distributed by Zydus Pharmaceuticals in New Jersey.*

* 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.