Nifedipine Tablet, Film Coated, Extended Release
Product Images NDC 51655-990

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 51655-990). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, Llc, 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

Label (51655 990 26 Master Bottle Label Approval Rev A 05 22)

Label (51655 990 26 Master Bottle Label Approval   Rev A 05 22)
Nifedipine Extended-release Tablets, USP, 30 mg, 90 count. The label shows the product name, strength, dosage form as film-coated extended-release tablets, and quantity. It includes storage instructions to keep at 20°-25°C (68°-77°F) and protect from moisture and humidity. The label states Rx only and lists Northwind Pharmaceuticals as the repacker and Northwind Pharmaceuticals LLC as the labeler.*
FDA Label Image

Structure (6dce3884 D5b6 4a52 A2e8 03d1de853aa2)

Structure (6dce3884 D5b6 4a52 A2e8 03d1de853aa2)
Chemical structure of nifedipine, showing its molecular arrangement with characteristic rings and functional groups including nitro and acetyl groups.*

* 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.