Nifedipine Tablet, Extended Release
Product Images NDC 50090-6450

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nifedipine (NDC 50090-6450). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

01 (Image 01)

Chemical structure of nifedipine, showing its molecular composition including a dihydropyridine ring with methyl, methoxycarbonyl, acetyl, and nitrophenyl substituents.*

FDA Label Image

02 (Image 02)

A data table comparing the percentage of adverse effects reported for nifedipine extended-release tablets (N=707) versus placebo (N=266). It lists headache, fatigue, dizziness, constipation, and nausea, showing higher percentages of headache and fatigue with nifedipine compared to placebo.*

FDA Label Image

03 (Image 03)

A data table presenting the percentage of adverse effects reported for Nifedipine capsules compared to placebo. The table lists specific adverse effects such as dizziness, flushing, headache, weakness, and others, with corresponding percentages for each group (Nifedipine N=226, Placebo N=235).*

FDA Label Image

Label Image (Lbl500906450)

Nifedipine 90 mg extended-release oral tablets label by A-S Medication Solutions. The label includes dosage form and strength, storage instructions to keep between 60 and 77 degrees Fahrenheit, and protection from moisture. It also states the package contains 30 tablets and includes space for dosage instructions and a barcode.*

* 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.