Loargys Injection
Product Images NDC 81583-105

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Loargys (NDC 81583-105). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Immedica Pharma Us 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

Figure 1 (Image 01)

A line chart comparing mean arginine levels (µM) over time between Loargys and placebo-Loargys groups, spanning baseline through a long-term extension period (LTE). The chart includes error bars, with separate lines for double-blind and LTE phases, showing Loargys decreasing arginine levels while placebo levels remain higher.*

FDA Label Image

Principal Display Panel (2 mg/0.4 mL Carton)

Loargys (pegzilarginase-nbln) Injection 2 mg/0.4 mL single-dose vial packaging label. For intravenous infusion after dilution or subcutaneous injection. Contains 5 mg pegzilarginase-nbln per mL. Manufactured by Immedica Pharma AB, Sweden, and marketed by Immedica Pharma US Inc., Chicago, IL. Includes storage instructions, dosage information references, and barcode.*

FDA Label Image

Principal Display Panel (5 mg/1 mL Carton)

Loargys 5 mg/mL injection label, containing pegzilarginase-nbln, for intravenous or subcutaneous administration. The label includes dosage instructions, storage conditions, and manufacturer information. The labeler is Immedica Pharma US Inc. and the product comes in a 1 mL single-dose vial. It lists the active ingredient concentration and excipients along with barcode and regulatory details.*

* 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.