Nifedipine Tablet, Extended Release
Product Images NDC 51655-798

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 51655-798). 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 798 26 Master Bottle Label Approval Rev A 02 22)

Label (51655 798 26 Master Bottle Label Approval   Rev A 02 22)
This is a prescription medicine called Nifedipine. It comes in extended-release tablets of 30mg and there are 90 tablets in a package. The tablets should be taken whole, without splitting or biting. It is kept in a container away from moisture and light at a temperature of 25°C (77°F), with excursions to 15°-30°C (55°-86°F). The lot number is 0000000000, and the medicine is repackaged by Northwind Pharmaceuticals. The expiration date is 00/00/0000. It contains nifedipine, USP 30mg. It is made by Bausch Health US, LLC and there is a caution label to keep it out of the reach of children.*
FDA Label Image

Nifedipine Chemical Structure (Nifedipine 01)

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