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Nifedipine Tablet, Extended Release
Product Images NDC 68382-687
View Photos of 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 68382-687). 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.
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This is a description of a medication package containing film-coated extended-release tablets for Nifedipine, USP. Each tablet has a dose of 33mg and is intended to provide a 30mg dose. The package is child-resistant and the tablets should be kept out of children's reach. It is recommended to store the tablets at 20° to 25°C (68° 0 77°F) and to protect them from moisture and humidity. The medication is manufactured by Cadia Healthcare Lid., in Anmedabad, India and is distributed by Zydus Pharmaceuticals USA Inc. This medication is only available through a prescription.*
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This is a label of a medication containing extended-release tablets of 60mg dose of 66mg of Fedipine, USP. It also contains information about dosage, child resistance, storage conditions, and manufacturing details. The medication is distributed by Zydus Pharmaceuticals in the USA, and the label contains a coding template with a non-printable, unvarnished area.*
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This is a label template for a medicine bottle. It contains information about the dosage and storage of extended-release tablets, which contain 99mg of nifedipine. The tablets come in a bottle of 100 and are dispensed by Cadia Healthcare Ltd. The label warns to keep the bottle out of reach of children and protect it from moisture and humidity. The medication requires protection from excessive heat and light exposure, and dosage instructions should be as listed on the package insert. The medicine is distributed by Zydus Pharmaceuticals (USA) Inc. The label bears a prescription-only warning.*
* 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.
