Spironolactone Tablet, Film Coated
Product Images NDC 63629-2438

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 63629-2438). 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 (Structure)

Structure (Structure)
Chemical structure of spironolactone, the active ingredient in Spironolactone 50 mg film-coated tablets by Bryant Ranch Prepack. The structure shows a multi-ring steroid backbone with ketone and thioester functional groups.*
FDA Label Image

Figure01 (Fig01)

Figure01 (Fig01)
A Kaplan-Meier survival curve comparing the probability of an outcome over 48 months between two groups: Spironolactone (n=822) and Placebo (n=841). The graph shows a higher probability for the Spironolactone group throughout the period, with a significance level indicated by a log-rank p-value of <0.001. The x-axis represents time in months, and the y-axis represents probability.*
FDA Label Image

Figure02 (Fig02)

Figure02 (Fig02)
A forest plot chart showing hazard ratios (HR) and 95% confidence intervals (CI) for various subgroups evaluating the effect of spironolactone versus placebo. Subgroups include age, sex, race, left ventricular ejection fraction (LVEF), heart failure type, NYHA class, diabetes status, serum creatinine, creatinine clearance, potassium levels, digoxin use, ACE inhibitor use, and beta blocker use. The x-axis ranges from 0.2 to 1.4, indicating whether spironolactone or placebo is favored.*
FDA Label Image

Label (Lbl636292438)

Label (Lbl636292438)
Label for Spironolactone Tablets, USP 50 mg oral film-coated tablets by Bryant Ranch Prepack. The label includes the NDC number 63629-2438-1, a barcode, quantity of 100 tablets, and instructions for storage and dispensing in a child-resistant container. The label displays the BRP Pharmaceuticals 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.