Nifedipine Tablet, Extended Release
Product Images NDC 51655-738

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Nifedipine (NDC 51655-738). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, Llc, 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

Label (51655 738 52 Master Bottle Label Approval Rev A 06 21)

Label (51655 738 52 Master Bottle Label Approval   Rev A 06 21)
NIFEdipine is available in an extended-release tablet form with a strength of 90 mg. The package comes with 30 tablets, and the dosage information is provided in the package insert. The medicine should be stored in its original container and protected from moisture and humidity. The drug should be kept away from children. The lot number is 0000000000, and the expiration date is listed as 00/00/0000. The drug is repackaged by Northwind Pharmaceuticals, and its label is 51655-738-52. The tablet is made up of 99 mg nifedipine, which provides a dose of 90 mg.*
FDA Label Image

Image Description (6d475a6d Figure 01)

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