Prednisone Tablet
Product Images NDC 72189-430

View Photos of 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 Prednisone (NDC 72189-430). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct_rx, 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

72189-430-10 (72189 430 10)

72189-430-10 (72189 430 10)
Prednisone 20 mg oral tablets packaged in a blister pack with 10 tablets per pack. The label indicates the generic name Deltasone and specifies each tablet contains 20 mg prednisone USP. The product is labeled by Direct_Rx with lot and expiration details visible. The package includes NDC code 72189-430-10.*
FDA Label Image

72189-430-20 (72189 430 20)

72189-430-20 (72189 430 20)
Prednisone 20 mg oral tablets packaging label from Direct_Rx. The label indicates 20 mg strength, 20 tablets per package, and states the generic for Deltasone. Lot number and expiration date (8/31/24) are visible, along with product and manufacturing details including NDC 72189-430-20.*
FDA Label Image

72189-430-21 (72189 430 21)

72189-430-21 (72189 430 21)
The image shows a prescription drug label for Prednisone 20 mg oral tablets by Direct Rx. The label highlights a package containing 21 tablets. It lists Prednisone as the generic for Deltasone and states each tablet contains 20 mg prednisone USP. The NDC number 72189-430-21 is visible, along with packaging and lot sample details including expiration date 8/31/24.*

* 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.