Nifedipine Tablet, Film Coated, Extended Release
Product Images NDC 60760-862

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Nifedipine (NDC 60760-862). 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

862-90 (Nifedipine 60760 862 90)

Nifedipine Extended-Release Tablets, USP 90 mg film-coated oral tablets in a 90-count package. Label shows product NDC 60760-862-90, manufactured by Ingenus Pharmaceuticals, LLC, and packaged by St. Mary's Medical Park Pharmacy in Oro Valley, AZ. Storage instructions specify controlled room temperature between 15°-30°C (59°-86°F).*

FDA Label Image

01 (Image 01)

Chemical structure of nifedipine, showing its molecular arrangement including nitro, acetoxy, and methyl groups attached to a dihydropyridine ring and a benzene ring.*

FDA Label Image

02 (Image 02)

A data table showing the percentage incidences of adverse effects in patients taking Nifedipine extended-release tablets (N=707) compared to placebo (N=266). Reported effects include headache, fatigue, dizziness, constipation, and nausea, with higher percentages generally observed in the Nifedipine group.*

FDA Label Image

03 (Image 03)

A data table comparing the percentage of patients experiencing various adverse effects with Nifedipine Capsules versus Placebo. It lists adverse effects such as dizziness, flushing, headache, weakness, nausea, muscle cramps, edema, nervousness, palpitations, dyspnea, and nasal congestion, showing reported percentages for each treatment group.*

FDA Label Image

04 (Image 04)

* 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.