Nifedipine Tablet, Extended Release
Product Images NDC 68382-685

4 FDA label images from Zydus Pharmaceuticals (usa) Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nifedipine (NDC 68382-685). 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 nifedipine, showing the molecular arrangement including a dihydropyridine ring with methyl, acetoxy, and nitrophenyl substituents.*
FDA Label Image

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Nifedipine Extended-Release Tablets 30 mg, bottle label by Zydus Pharmaceuticals (USA) Inc. The label displays the NDC 68382-685-01 and packaging size of 100 tablets. It includes storage instructions, dosing note, and manufacturer details: Cadila Healthcare Ltd., Ahmedabad, India, with distribution by Zydus Pharmaceuticals (USA) Inc., Pennington, NJ.*
FDA Label Image

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Label for Nifedipine Extended-Release Tablets 60 mg by Zydus Pharmaceuticals, showing a 100-tablet package for oral use. The label includes dosing information, storage instructions, and distributor details for Zydus Pharmaceuticals (USA) Inc. The product is prescription-only and child-resistant.*
FDA Label Image

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Nifedipine Extended-Release Tablets 90 mg, oral extended-release tablets in a package of 100 tablets. The label notes child-resistant packaging, storage instructions, and the prescription-only status. Manufactured by Cadila Healthcare Ltd., India, and distributed by Zydus Pharmaceuticals (USA) Inc., Pennington, NJ.*

* 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.