Finasteride Tablet, Film Coated
Product Images NDC 57237-061

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Finasteride (NDC 57237-061). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rising Pharma Holdings, 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

Figure 1 (Finasteride Fig1)

Figure 1 (Finasteride Fig1)
A line graph depicting the effect on hair count measured as the mean change in number of hairs within a 1-inch diameter circle from baseline over a period of 5 years. The graph compares finasteride 1 mg and placebo, showing distinct trends with data points and sample sizes for each time interval. This chart illustrates hair count changes related to finasteride versus placebo based on pooled data from vertex hair loss studies.*
FDA Label Image

Package Label-principal Display Panel (1 mg (30 Tablet Bottle))

Package Label-principal Display Panel (1 mg (30 Tablet Bottle))
Finasteride Tablets USP 1 mg film-coated tablets label from Rising Pharma Holdings, Inc. The label states the product contains 30 tablets with a prescription-only designation, dosage of 1 mg once daily, and storage instructions. It also includes warnings about use by women and children, distributor information for Rising Health, LLC, and origin marked as Made in India.*
FDA Label Image

Chemical Structure (Finasteride Str)

Chemical Structure (Finasteride Str)
Chemical structure of finasteride, depicting its molecular framework including ring systems and functional groups.*

* 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.