Spironolactone Tablet
Product Images NDC 72162-1624

View Photos of 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 72162-1624). 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

Structure (Spironolactone 01)

Structure (Spironolactone 01)
Chemical structure diagram of spironolactone showing its molecular framework, including steroid backbone and functional groups such as a lactone ring and thioester moiety.*
FDA Label Image

Figure 1 (Spironolactone 02)

Figure 1 (Spironolactone 02)
A line graph comparing the probability over time in months for two groups: Spironolactone (n=822) and placebo (n=841). The graph shows a higher probability for the placebo group across the months, with a statistically significant difference (Log-rank p < 0.001).*
FDA Label Image

Figure 2 (Spironolactone 03)

Figure 2 (Spironolactone 03)
A forest plot figure displaying hazard ratios (HR) with 95% confidence intervals (CI) for various subgroups related to age, sex, race, LVEF percentage, heart failure type, NYHA class, diabetes status, serum creatinine levels, creatinine clearance, potassium levels, digoxin, ACE inhibitor, and beta blocker use. The x-axis ranges from 0.2 to 1.4, indicating the relative benefit of spironolactone versus placebo across different subgroups.*
FDA Label Image

Label (Lbl721621624)

Label (Lbl721621624)
Label for Spironolactone Tablets, USP 25 mg oral tablets, 100 count. The product is repackaged by Bryant Ranch Prepack, Inc., Burbank, CA, and manufactured by Frontida BioPharm, Inc. The label includes storage instructions (20° to 25°C), a warning to keep out of reach of children, and to dispense in a tight, light-resistant container. The NDC is 72162-1624-1.*

* 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.