Nifedipine
Product Images NDC 53808-0389

3 FDA label images from State Of Florida Doh Central Pharmacy · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Nifedipine (NDC 53808-0389). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by State Of Florida Doh Central 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

Label Image For 30mg (Nifedipine Er 30mg(actavis))

Label Image For 30mg (Nifedipine Er 30mg(actavis))
Nifedipine ER 30 mg tablet packaging label showing quantity of 30 tablets. Label includes lot number PF3580151A, expiration date August 2010, and packaging by DOH Central Pharmacy, Tallahassee, FL 32304. Barcode and UPC number 367767153012 are visible. The label notes "RX Only" and the manufacturer as Actavis.*
FDA Label Image

Label Image For 60mg (Nifedipine Er60mg(actavis))

Label Image For 60mg (Nifedipine Er60mg(actavis))
Packaging label for Nifedipine ER 60 mg tablet with a quantity of 30 tablets. The label includes lot number PF3590150A and expiry date 063010. It is packaged by DOH Central Pharmacy, labeled by State of Florida DOH Central Pharmacy in Tallahassee, FL 32304. A UPC barcode is also visible.*
FDA Label Image

Molecular Structure (Nifedipine Er Tab 01)

Molecular Structure (Nifedipine Er Tab 01)
Chemical structure diagram of Nifedipine depicting its molecular arrangement with labeled chemical groups and bonds, corresponding to the active ingredient Nifedipine.*

* 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.