Spironolactone Tablet, Film Coated
Product Images NDC 72162-1693

4 FDA label images from Bryant Ranch Prepack · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Spironolactone (NDC 72162-1693). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Image Description (Structure)

Image Description (Structure)
Chemical structure of the active ingredient spironolactone, depicted as a molecular diagram showing multiple rings and functional groups typical of its steroid-like structure.*
FDA Label Image

Image Description (Figure 1)

Image Description (Figure 1)
A survival curve graph depicting probability over time (months) comparing Spironolactone with placebo. The y-axis shows probability while the x-axis represents time in months. The graph includes two lines: one for Spironolactone (n=822) and one for placebo (n=841). Statistical significance is indicated with a log-rank p-value less than 0.001.*
FDA Label Image

Image Description (Figure 2)

Image Description (Figure 2)
A forest plot chart showing hazard ratios (HR) and 95% confidence intervals (CI) for different subgroups in a clinical study comparing Spironolactone 25 mg film coated tablets to placebo. Subgroups include age, sex, race, LVEF, heart failure type, NYHA class, diabetes status, serum creatinine, creatinine clearance, potassium level, and use of digoxin, ACE inhibitors, or beta blockers.*
FDA Label Image

Label (Lbl721621693)

Label (Lbl721621693)
The label for Spironolactone Tablets USP 25 mg shows a film-coated oral tablet formulation. The package contains 500 tablets. It is labeled by Bryant Ranch Prepack, Inc., Burbank, CA, and manufactured by Jubilant Generics Limited. The label includes storage instructions, safety warnings, and two barcodes along with the NDC number 72162-1693.*

* 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.