Megestrol Acetate Suspension
Product Images NDC 68094-063

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Megestrol Acetate (NDC 68094-063). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Precision Dose 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

Chemical Structure (Megestrol 01)

Chemical Structure (Megestrol 01)
Chemical structure diagram of Megestrol Acetate showing its steroid backbone with multiple attached methyl and acetoxy groups, depicted with rings and bond lines.*
FDA Label Image

Trial 1 (Megestrol 02)

Trial 1 (Megestrol 02)
A line graph labeled 'Trial 1' showing mean weight change in pounds over time in weeks. The x-axis indicates weeks from 0 to 12, and the y-axis shows mean weight change from -3 to 12 pounds. Four treatment groups are represented with different dosage levels: 800 mg, 400 mg, 100 mg, and placebo. Weight change increases most with 800 mg and least with placebo over the trial period.*
FDA Label Image

Trial 2 (Megestrol 03)

Trial 2 (Megestrol 03)
A line graph titled Trial 2 depicting mean weight change (in pounds) over 12 weeks. The x-axis represents time in weeks (0, 4, 8, 12) and the y-axis shows mean weight change ranging from -3 to 12 pounds. Two lines compare an 800 mg dosage group and a placebo group, with the 800 mg group showing increasing weight gain and the placebo group showing a slight decrease over time.*
FDA Label Image

Principal Display Panel (10 mL Cup Label)

Principal Display Panel (10 mL Cup Label)
Label for Megestrol Acetate Oral Suspension, USP 400 mg/10 mL (equivalent to 40 mg/mL) by Precision Dose Inc. The label includes storage instructions to keep between 20-25°C (68-77°F) and protect from heat. It notes the alcohol content as a maximum of 0.06% v/v and advises shaking well before dosing. The label also features the NDC number 68094-063-59 and the manufacturer's location in South Beloit, IL.*

* 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.