Angeliq
Product Images NDC 54868-6184

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Angeliq (NDC 54868-6184). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physicians Total Care, 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

Structural Formula (B9996465 177a 49cf A6c1 Be5a44addde9 01)

Chemical structure of Drospirenone and Estradiol as active ingredients. The image shows molecular diagrams of Drospirenone and Estradiol 1/2 H2O associated with the product Angeliq by Physicians Total Care, Inc.*

FDA Label Image

Figure 1 (B9996465 177a 49cf A6c1 Be5a44addde9 02)

A line graph showing mean serum concentrations of drospirenone and estradiol over 24 hours after dosing. The x-axis represents time in hours, and the y-axes represent drospirenone concentration in ng/mL (left) and estradiol concentration in pg/mL (right). Drospirenone levels peak early and decline steadily, while estradiol levels show a different profile with a secondary plateau.*

FDA Label Image

Figure 2 (B9996465 177a 49cf A6c1 Be5a44addde9 03)

Line graph showing percent values over 13 cycles comparing two groups: E2 1 mg and E2 + DRSP 0.5 mg. The graph plots percent on the vertical axis against cycle number on the horizontal axis, indicating trends in percent changes across cycles for both treatment groups.*

FDA Label Image

Angeliq Package Label (Package Label)

Angeliq 0.5/1 mg tablet label distributed by Physicians Total Care, Inc., Tulsa, OK. The label displays the NDC 54868-6184-0, lot number 000, and an expiration date of 01/60. It includes a barcode and states manufacturing by Bayer Healthcare Pharmaceuticals, Wayne, NJ 07470.*

* 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.