Paricalcitol Injection
Product Images NDC 55150-215

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Paricalcitol (NDC 55150-215). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eugia Us Llc, 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

A Long-term, Open-label Safety Study Of 164 Ckd Stage 5 Patients (Paricalcitol Fig1)

Label for Paricalcitol Injection USP, 2 mcg per mL, 1 mL single dose vial by Eugia US LLC. The label states it is for intravenous use, contains 20% alcohol, and is manufactured in India for AuroMedis Pharma LLC, E. Windsor, NJ. NDC 55150-212-01 is visible along with a barcode and a QR code.*

FDA Label Image

Package Label-principal Display Panel – 2 Mcg/ml Container Label (Paricalcitol Fig2)

Paricalcitol Injection, USP 2 mcg per mL intravenous injection, sterile, presented in a carton for 25 single-dose 1 mL vials. The label shows the distributor as AuroMedics Pharma LLC and indicates storage conditions and aseptic technique instructions. The product is manufactured in India and labeled for prescription use only.*

FDA Label Image

Package Label-principal Display Panel (2 mcg/mL Container-Carton (25 Vials))

Label of Paricalcitol Injection, USP 5 mcg per mL from Eugia US LLC, showing a single dose vial of 1 mL for intravenous use. The label states it contains 20% alcohol, is manufactured in India for AuroMedis Pharma LLC, and includes barcodes and a QR code.*

FDA Label Image

Package Label-principal Display Panel – 5 Mcg/ml Container Label (Paricalcitol Fig4)

Packaging label for Paricalcitol Injection, USP 5 mcg per mL sterile intravenous injection. The label indicates a package containing 25 single-dose 1 mL vials. Distributed by AuroMedics Pharma LLC, the label includes storage and handling instructions as well as the NDC 55150-213-01.*

FDA Label Image

Package Label-principal Display Panel (5 mcg/mL Container-Carton (25 Vials))

Paricalcitol Injection, USP 10 mcg per 2 mL (5 mcg/mL) vial label for intravenous use, single dose, 2 mL. The label includes the statement 'Contains alcohol, 20% (v/v)' and indicates manufacturing by AuroMedis Pharma LLC for Eugia US LLC, located in E. Windsor, NJ. Includes barcode and QR code.*

FDA Label Image

Package Label-principal Display Panel – 10 Mcg/2 mL (5 Mcg/ml) [single Dose Vial] (Container Label)

Paricalcitol Injection, USP 10 mcg per 2 mL (5 mcg/mL) in single-dose vials, labeled for intravenous use. The sterile package contains 25 vials of 2 mL each. Distributed by AuroMedics Pharma LLC, with a manufacturing origin noted as India. The label includes storage instructions and mentions the vial stoppers are not made with natural rubber latex.*

FDA Label Image

Package Label-principal Display Panel (10 mcg/2 mL (5 mcg/mL) [Single Dose Vial])

Paricalcitol Injection, USP 10 mcg per 2 mL (5 mcg/mL) in a 2 mL multiple-dose vial. For intravenous use. Label indicates 20% alcohol content and that it is manufactured in India for AuroMedis Pharma LLC. NDC 55150-215-02, labeled by Eugia US LLC.*

FDA Label Image

Package Label-principal Display Panel – 10 Mcg/2 mL (5 Mcg/ml) [multi Dose Vial] (Container Label)

Packaging label for Paricalcitol Injection, USP 10 mcg per 2 mL (5 mcg/mL) intravenous injection. The multiple-dose vial contains 25 vials of 2 mL each. The label shows the Rx only designation, sterility, Auromedics branding, and storage instructions. Distributed by AuroMedics Pharma LLC.*

FDA Label Image

Paricalcitol Chemical Structure (Paricalcitol Str)

Chemical structure of paricalcitol, illustrating its molecular framework with hydroxyl groups and double bonds characteristic of the active ingredient in the PARICALCITOL injection product by Eugia US LLC.*

* 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.