Nifedipine Tablet, Extended Release
Product Images NDC 70771-1192

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nifedipine (NDC 70771-1192). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences Limited, 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 diagram of Nifedipine, showing its molecular framework including aromatic rings, nitro group, and ester functional groups.*

FDA Label Image

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Nifedipine Extended-Release Tablets 30 mg label showing an oral tablet dosage form with a beige round tablet marked "685". The label includes the NDC 70771-1190-1 and states a package size of 100 tablets. Manufactured by Cadila Healthcare Ltd., Matoda, Ahmedabad, India, and labeled by Zydus Lifesciences Limited. The label also displays storage instructions and a safety warning to keep out of reach of children.*

FDA Label Image

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Nifedipine Extended-Release Tablets 60 mg, oral extended-release tablets, packaged in a bottle count of 100, manufactured by Cadila Healthcare Ltd., Matoda, Ahmedabad, India. The label features a depiction of a single tan round tablet imprinted with '686'. The label also displays the NDC 70771-1191-1 and includes storage and dispensing instructions.*

FDA Label Image

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Label for Nifedipine Extended-Release Tablets, 90 mg strength. The label shows a brown colored round tablet imprinted with '687'. The package contains 100 tablets and is for oral use. The labeler is Zydus Lifesciences Limited, with manufacturing by Cadila Healthcare Ltd., Ahmedabad, India. The label includes storage and dispensing instructions along with a barcode and NDC 70771-1192-1.*

* 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.