Nifedipine Tablet, Film Coated, Extended Release
Product Images NDC 71335-1721

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Nifedipine (NDC 71335-1721). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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 framework with two aromatic rings, nitro group, methoxy groups, and keto functional groups.*

FDA Label Image

02 (Image 02)

A data table comparing the percentage of adverse effects reported with Nifedipine extended-release tablets (N=707) versus placebo (N=266). Adverse effects listed include headache, fatigue, dizziness, constipation, and nausea with corresponding percentages for each group.*

FDA Label Image

03 (Image 03)

A data table comparing the percentage of patients experiencing various adverse effects between Nifedipine capsules (N=226) and placebo (N=235). Adverse effects listed include dizziness, flushing, headache, weakness, nausea, muscle cramps, peripheral edema, nervousness, palpitations, dyspnea, and nasal congestion, with percentages varying between the two groups.*

FDA Label Image

04 (Image 04)

FDA Label Image

Label (Lbl713351721)

Nifedipine ER 60 mg Tablet film-coated extended release oral dosage form label. Packaged by Bryant Ranch Prepack, Burbank, CA. The label compares to Procardia ER 60 mg Tablet by Novast Laboratories. The packaging has a lot number and storage instructions at room temperature (20°-25°C). The label includes warnings to keep drugs out of children’s reach, NDC 71335-1721, 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.