Ella
Product Images NDC 53002-1630

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ella (NDC 53002-1630). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rpk Pharmaceuticals, 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

Ulipristal Acetate Structural Formula (Ella Tablet 1)

Ulipristal Acetate Structural Formula (Ella Tablet 1)
Chemical structure of the active ingredient in Ella, a pharmaceutical product by RPK Pharmaceuticals, Inc. The diagram shows the molecular formula with rings, functional groups, and stereochemistry typical of its active compound.*
FDA Label Image

Figure 1: Mean ((± Sd) Plasma Concentration-time Profile Of Ulipristal Acetate And Monodemethyl-ulipristal Acetate Following Single Dose Administration Of 30 mg Ulipristal Acetate (Ella Tablet 2)

Figure 1: Mean ((± Sd) Plasma Concentration-time Profile Of Ulipristal Acetate And Monodemethyl-ulipristal Acetate Following Single Dose Administration Of 30 mg Ulipristal Acetate (Ella Tablet 2)
A pharmacokinetic curve showing the concentration (ng/mL) of ulipristal acetate and monodemethyl-ulipristal acetate in blood plasma over time (hours). Concentrations for both substances decrease over a 168-hour period, with ulipristal acetate maintaining higher levels than monodemethyl-ulipristal acetate throughout.*
FDA Label Image

Label Image (Lbl530021630)

Label Image (Lbl530021630)
Label for Ella 30 mg tablet by RPK Pharmaceuticals, Inc. The label indicates a single dose of one tablet. It includes the active ingredient ulipristal acetate and the product NDC 53002-1630. Various barcodes, lot number, and expiration date details are visible on the label.*

* 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.