Nifedipine Tablet, Extended Release
Product Images NDC 59651-296

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nifedipine (NDC 59651-296). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma 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

Package Label-principal Display Panel (30 mg (100 Tablets Bottle))

Nifedipine Extended-Release Tablets USP 30 mg film-coated extended-release tablets, labeled for 100 tablets per container. Distributed by Aurobindo Pharma USA, Inc., made in India. Includes storage and handling instructions, dosage form as extended-release oral tablets, and product label details such as NDC 59651-295-01 and bar code.*

FDA Label Image

Package Label-principal Display Panel (60 mg (100 Tablets Bottle))

Label for NIFEdipine Extended-Release Tablets USP, 60 mg strength, in a bottle containing 100 tablets. The label states the product is prescription only and film-coated with extended release. It includes storage instructions and distributor details for Aurobindo Pharma USA, Inc., with production made in India by Aurobindo Pharma Limited.*

FDA Label Image

Package Label-principal Display Panel (90 mg (100 Tablets Bottle))

Nifedipine Extended-Release Tablets, USP 90 mg film-coated tablets, supplied in a package containing 100 tablets. The label shows dosage form as extended-release tablets for oral use. The product is distributed by Aurobindo Pharma USA, Inc., and manufactured in India by Aurobindo Pharma Limited. Storage instructions, prescription status, and packaging details are noted.*

FDA Label Image

Chemical Strucure (Nifedipine Str)

Chemical structure of Nifedipine, showing its molecular arrangement with nitro, methoxy, acetyl, and dimethylamino groups attached to a dihydropyridine ring and a benzene ring.*

* 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.