Nifedipine Tablet, Extended Release
Product Images NDC 60760-859

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Nifedipine (NDC 60760-859). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by St. Mary's Medical Park Pharmacy, 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

859-90 (Nifedipine 60760 859 90)

FDA Label Image

01 (Image 01)

FDA Label Image

02 (Image 02)

02 (Image 02)
This table displays the adverse effects reported by individuals taking Nifedipine extended-release tablets compared to a placebo. The adverse effects include headache, fatigue, dizziness, constipation, and nausea. The percentage of individuals experiencing these side effects is provided for both Nifedipine and placebo groups.*
FDA Label Image

03 (Image 03)

03 (Image 03)
This table presents the comparison of adverse effects experienced by individuals taking nifedipine capsules versus those who took a placebo. The total number of participants in each group is provided within parentheses. Some of the reported adverse effects and their respective percentages for both groups include dizziness, lightheadedness, giddiness (27% nifedipine vs. 15% placebo), flushing, heat sensation (25% nifedipine vs. 8% placebo), headache (23% nifedipine vs. 20% placebo), weakness (12% nifedipine vs. 10% placebo), and more. The comparison indicates the incidence rates of each adverse effect to help evaluate the differences between the two groups.*
FDA Label Image

04 (Image 04)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.