Paricalcitol Capsule
Product Images NDC 72162-1916

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Paricalcitol (NDC 72162-1916). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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 (Lbl721621916)

Label for Paricalcitol Capsules 2 mcg strength, containing 30 capsules. The label shows the NDC 72162-1916-3 and states the capsules contain 2 mcg Paricalcitol, USP and 1.2% alcohol, USP dehydrated. It is labeled by Bryant Ranch Prepack, Inc. and manufactured by Patheon Softgels Inc. Storage instructions and warnings are included.*

FDA Label Image

Structural Formula (Paricalcitol 01)

Chemical structure of paricalcitol, showing its molecular formula with multiple rings and hydroxyl groups visible in the diagram.*

FDA Label Image

Figure 1 (Paricalcitol 02)

A line graph comparing iPTH levels (pg/mL) over 23 weeks between Paricalcitol and placebo groups. The solid line represents Paricalcitol, showing a downward trend in iPTH levels, while the dashed line represents placebo, showing relatively stable or slightly increasing iPTH levels. Time is shown on the x-axis in weeks.*

FDA Label Image

Figure 2 (Paricalcitol 03)

A line graph comparing serum iPTH levels (pg/mL) over 12 weeks between Paricalcitol and placebo groups. The Y-axis shows iPTH concentration from 100 to 1100 pg/mL, and the X-axis shows time in weeks. Paricalcitol group shows a decline and stabilization in iPTH, whereas placebo group shows a slight increase. Error bars indicate variability at each time point.*

* 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.