Premarin
Product Images NDC 53808-0770

3 FDA label images from State Of Florida Doh Central Pharmacy · 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 Premarin (NDC 53808-0770). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by State Of Florida Doh Central Pharmacy, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Principal Display Panel (0.625 mg)

Principal Display Panel (0.625 mg)
Premarin 0.625 mg tablet label showing prescription-only status, quantity of 30 tablets, lot number 186477A, expiration date 09/30/2010, and packaging by DOH Central Pharmacy in Tallahassee, FL. Includes barcode and UPC number 300461102818.*
FDA Label Image

Figure 1 (Premarin Tablets 01)

Figure 1 (Premarin Tablets 01)
A cumulative distribution curve graph showing the percent change from baseline in spine bone mineral density (BMD) on the x-axis versus the cumulative percent of subjects on the y-axis. Four different lines represent groups labeled 0.625, 0.45, 0.3, and placebo, comparing their changes in spine BMD over time.*
FDA Label Image

Figure 2 (Premarin Tablets 02)

Figure 2 (Premarin Tablets 02)
A line graph showing adjusted percent change from baseline on the Y-axis and cycle number on the X-axis, comparing four groups labeled 0.625, 0.45, 0.3, and placebo. Each group is represented by different symbols and lines, with sample sizes indicated in a legend within the graph. The graph includes error bars for each data point over multiple cycles.*

* 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.