Nifedipine Tablet, Film Coated, Extended Release
Product Images NDC 68788-7642

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Nifedipine (NDC 68788-7642). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Preferred Pharmaceuticals, Inc., 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 diagram of nifedipine, showing its molecular configuration including aromatic rings, nitro group, and ester functional groups, consistent with the nifedipine molecule.*

FDA Label Image

02 (Image 02)

A table presenting the percentage of adverse effects in subjects taking Nifedipine extended-release tablets compared to placebo. It lists headache, fatigue, dizziness, constipation, and nausea with respective occurrence percentages for 707 subjects on Nifedipine and 266 subjects on placebo.*

FDA Label Image

03 (Image 03)

A table comparing the percentage of subjects reporting various adverse effects while taking Nifedipine extended-release tablets (30 mg) versus placebo. The adverse effects listed include dizziness, flushing, headache, weakness, nausea, muscle cramps, peripheral edema, nervousness, palpitations, dyspnea, and nasal congestion, with respective percentages for each group.*

FDA Label Image

04 (Image 04)

FDA Label Image

Nifedipine Extended Release Tablet Usp 30mg (Image 05)

Nifedipine Extended-Release tablet, USP 30 mg, film-coated and extended-release dosage form. The label states it is a generic for Procardia XL and produced by Ingenus Pharmaceuticals, LLC. It includes storage instructions, warnings, and spaces for lot and expiration dates. The label features both English and Spanish directions for use with a bright yellow background and black and blue text.*

* 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.