Finasteride Tablet, Film Coated
Product Images NDC 35573-400

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Finasteride (NDC 35573-400). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Burel Pharmaceuticals, Llc, 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

Figure 1 (Finasteride Fig1)

A line graph titled 'Effect on Hair Count' showing the mean change in number of hairs within a 1-inch diameter circle from baseline over a 5-year period. The y-axis represents mean change in hairs from baseline (ranging approximately from -275 to 125), and the x-axis shows time points from baseline through 5 years. Four groups are plotted with distinct markers indicating different treatments: finasteride 1 mg and placebo, with data pooled from vertex hair loss studies. The graph includes error bars representing ±1 standard error and sample sizes (N) for each group at each time point.*

FDA Label Image

Package Label-principal Display Panel (1 mg (1000 Tablet Bottle))

Label for Finasteride Tablets USP 1 mg film-coated tablets in a package of 1,000 tablets. The label shows the product name, strength, dosage form, and manufacturer information including Burel Pharmaceuticals, LLC (Mason, OH) and Aurobindo Pharma Limited (Hyderabad, India). The label also displays warnings, storage conditions, and a barcode.*

FDA Label Image

Chemical Structure (Finasteride Str)

Chemical structure of finasteride, depicting its molecular framework including rings, methyl groups, and functional groups consistent with the active pharmaceutical ingredient finasteride.*

* 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.