Prednisone Delayed Release Tablet, Delayed Release
Product Images NDC 43598-888

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Prednisone Delayed Release (NDC 43598-888). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Reddys Laboratories Inc., 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

Carton5mg (Carton5mg)

Packaging label for Prednisone delayed release tablets, 5 mg strength, by Dr. Reddys Laboratories Inc. The label includes dosage form as delayed-release tablets with instructions to swallow whole and warnings not to crush, divide, or chew. The package contains 30 tablets and displays the NDC 43598-888-30 and storage temperature guidance.*

FDA Label Image

Chemical-structure (Chemical Structure)

Chemical structure diagram of prednisone, showing its steroidal four-ring core with hydroxyl, ketone, and methyl functional groups.*

FDA Label Image

Figure1 (Figure1)

A line graph showing prednisone plasma concentration (ng/mL) over time (hours) after oral administration of 5 mg prednisone delayed-release tablets under three conditions: fasting, semi-fed, and fed. Concentration peaks occur at different times depending on feeding state, with error bars indicating variability in measurements.*

FDA Label Image

Figure2 (Figure2)

A line graph comparing ACR20 responder percentages over 12 weeks between two groups: Prednisone delayed-release tablets plus DMARD and Placebo plus DMARD. The graph shows higher responder rates in the Prednisone group at all time points with data points at 0, 2, 6, and 12 weeks.*

FDA Label Image

Logo (Logo)

* 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.