Nifedipine Tablet, Extended Release
Product Images NDC 50090-6201

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nifedipine (NDC 50090-6201). 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)

01 (Image 01)
Chemical structure of nifedipine, illustrating its molecular configuration with labeled chemical groups and bonds as depicted in the image.*
FDA Label Image

02 (Image 02)

02 (Image 02)
A data table comparing the percentage incidence of adverse effects in patients taking nifedipine extended-release tablets (N=707) versus those taking placebo (N=266). Reported adverse effects include headache, fatigue, dizziness, constipation, and nausea, with the percentages listed for each group.*
FDA Label Image

03 (Image 03)

03 (Image 03)
A data table comparing the percentage of various adverse effects observed in groups taking Nifedipine capsules versus placebo. The adverse effects listed include dizziness, flushing, headache, weakness, nausea, muscle cramps, edema, mood changes, palpitations, respiratory symptoms, and nasal congestion with the number of participants noted for each group.*
FDA Label Image

Label Image (Lbl500906201)

Label Image (Lbl500906201)
Nifedipine 60 mg extended-release oral tablets packaging label from A-S Medication Solutions, Libertyville, Illinois. The label indicates 30 tablets, extended release, with storage instructions to keep at 68 to 77 degrees Fahrenheit, protected from light and moisture. NDC is 50090-6201-0.*

* 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.