Premarin Tablet, Film Coated
Product Images NDC 50090-1853

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Premarin (NDC 50090-1853). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

Label Image (Lbl500901853)

PREMARIN 0.3 mg film-coated tablets by A-S Medication Solutions. The label indicates each tablet contains 0.3 mg of conjugated estrogens, naturally occurring substances from the urine of pregnant mares. The package contains 30 tablets, with storage instructions to keep between 15 to 30 degrees Celsius (59 to 77 degrees Fahrenheit). The product NDC is 50090-1853.*

FDA Label Image

Figure 1 (Premarin 01)

A cumulative percentage curve graph depicting percent change from baseline in spine bone mineral density (BMD) among subjects. The graph shows four lines representing treatment groups with different dosages (0.625 mg, 0.45 mg, 0.3 mg) and a placebo group, illustrating changes over time or dosage with percent change on the x-axis and cumulative percent of subjects on the y-axis.*

FDA Label Image

Figure 2 (Premarin 02)

A line graph showing adjusted percent change from baseline over multiple cycles (up to 26) for various groups including different dose levels and a placebo. The graph plots the progression of measurements with error bars for each data point, illustrating trends for the different categories over time.*

FDA Label Image

Logo (Premarin 03)

FDA Label Image

Logo (Premarin 04)

* 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.