Finasteride
Product Images NDC 50436-0455

3 FDA label images from Unit Dose Services · 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 50436-0455). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unit Dose Services, 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

Finasteride-figure1 (Finasteride Figure1)

Finasteride-figure1 (Finasteride Figure1)
A line graph titled 'Effect on Hair Count' showing the mean change in the number of hairs in a 1-inch diameter circle from baseline over time. The graph includes data from baseline up to 5 years, comparing finasteride 1 mg and placebo groups with sample sizes noted at each time point. The Y-axis measures mean change in hairs from baseline, ranging from -275 to 125. The graph presents pooled data from vertex hair loss studies with mean change ± 1 standard error.*
FDA Label Image

Finasteride-structure (Finasteride Structure)

Finasteride-structure (Finasteride Structure)
Chemical structure of finasteride, showing its steroidal backbone with functional groups including a lactam ring and a tert-butyl amide moiety.*
FDA Label Image

Label Image (Lbl504360455)

Label Image (Lbl504360455)
Finasteride 1 mg film-coated tablets, 30 count packaging label from Unit Dose Services. The label includes dosage strength (1 mg), tablet count (30 tablets), and manufacturer information for Akelm Laboratories Ltd, Mumbai, India. It also contains storage instructions, warning not to use by women or children, and barcode with NDC 50436-0455-1. The product is labeled RX only and features lot and expiration date placeholders.*

* 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.