Nifedipine Tablet, Film Coated, Extended Release
Product Images NDC 0904-7208

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Nifedipine (NDC 0904-7208). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, 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

Structure (6dce3884 D5b6 4a52 A2e8 03d1de853aa2)

Structure (6dce3884 D5b6 4a52 A2e8 03d1de853aa2)
Chemical structure of Nifedipine, showing its molecular arrangement with nitro and acetyl functional groups attached to a dihydropyridine ring and benzene ring.*
FDA Label Image

Carton Label (B885b6b5 71c6 4799 8b23 5ee8c17938a0 00)

Carton Label (B885b6b5 71c6 4799 8b23 5ee8c17938a0 00)
Nifedipine Extended-Release Tablets, USP 30 mg film-coated extended-release oral tablets by Major Pharmaceuticals. The label indicates the product is for prescription use only, available in a package of 100 tablets. Storage and handling instructions, as well as manufacturer and distributor information, are provided on the label.*

* 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.