Baclofen Tablet
Product Images NDC 70710-1285

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Baclofen (NDC 70710-1285). 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 Baclofen showing a benzene ring with a chlorine atom and a side chain containing amino and carboxyl groups.*

FDA Label Image

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Baclofen Tablets USP 10 mg oral tablets packaging label from Zydus Pharmaceuticals. The label includes dosing instructions reference, storage conditions, and safety warnings. It shows the NDC number 70710-1285-1 and indicates the package contains 100 tablets. The label also identifies Cadila Healthcare Ltd. as the manufacturer and Zydus Pharmaceuticals (USA) Inc. as the distributor.*

FDA Label Image

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Label for Baclofen Tablets USP 20 mg oral tablets, packaged as 100 tablets. The label includes the NDC number 70710-1286-1 and states Rx only. It features storage instructions, manufacturer Cadila Healthcare Ltd. India, and distributor Zydus Pharmaceuticals (USA) Inc. The label shows branding with the zydus logo and includes a barcode.*

FDA Label Image

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Label for Baclofen Tablets, USP 5 mg oral tablets, containing 100 tablets per package. The label indicates prescription use only, with storage instructions at 20° to 25°C and cautions to keep the drug out of children's reach. It lists Cadila Healthcare Ltd. as the manufacturer and Zydus Pharmaceuticals (USA) Inc. as the distributor. The label includes the NDC 70710-1609-1 and a barcode.*

* 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.