Milrinone Lactate Injection, Solution
Product Images NDC 55150-287

7 FDA label images from Eugia Us Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Milrinone Lactate (NDC 55150-287). 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

Package Label-principal Display Panel (20 mg per 100 mL (200 mcg (0.2 mg) / mL))

Package Label-principal Display Panel (20 mg per 100 mL (200 mcg (0.2 mg) / mL))
Label for Milrinone Lactate in 5% Dextrose Injection, 20 mg per 100 mL (0.2 mg/mL) intravenous infusion solution. The label specifies it is a sterile, single-dose 100 mL flexible container. It includes usage instructions, cautions, storage recommendations, NDC 55150-287-01, and distributor information: AuroMedics Pharma LLC.*
FDA Label Image

Package Label-principal Display Panel (20 mg per 100 mL (200 mcg (0.2 mg) / mL))

Package Label-principal Display Panel (20 mg per 100 mL (200 mcg (0.2 mg) / mL))
Label for Milrinone Lactate in 5% Dextrose Injection, 20 mg per 100 mL (0.2 mg/mL) in a 100 mL single dose flexible container for intravenous infusion. The label indicates the product is sterile, Rx only, and includes handling and storage instructions. Distributed by AuroMedics Pharma LLC, made in India.*
FDA Label Image

Package Label-principal Display Panel (20 mg per 100 mL (200 mcg (0.2 mg) / mL))

Package Label-principal Display Panel (20 mg per 100 mL (200 mcg (0.2 mg) / mL))
Milrinone Lactate in 5% Dextrose Injection 0.2 mg/mL solution in 10 x 100 mL single dose flexible containers. The label indicates a concentration of 20 mg per 100 mL (200 mcg/mL). It is for intravenous infusion only and distributed by AuroMedics Pharma LLC. The label includes storage instructions and a caution about using only clear solutions.*
FDA Label Image

Package Label-principal Display Panel (40 mg per 200 mL (200 mcg (0.2 mg) / mL))

Package Label-principal Display Panel (40 mg per 200 mL (200 mcg (0.2 mg) / mL))
Label for Milrinone Lactate in 5% Dextrose Injection, 40 mg per 200 mL (0.2 mg/mL) solution for intravenous infusion. The sterile, single-dose flexible container label includes usage instructions, storage conditions, and distributor information for AuroMedics Pharma LLC.*
FDA Label Image

Package Label-principal Display Panel (40 mg per 200 mL (200 mcg (0.2 mg) / mL))

Package Label-principal Display Panel (40 mg per 200 mL (200 mcg (0.2 mg) / mL))
Milrinone Lactate in 5% Dextrose Injection label for a 200 mL single dose flexible container, with a concentration of 40 mg per 200 mL (0.2 mg/mL). The label indicates the product is sterile and for intravenous infusion only. It includes storage instructions, usage warnings, and distributor information for AuroMedics Pharma LLC. The product is made in India.*
FDA Label Image

Package Label-principal Display Panel (40 mg per 200 mL (200 mcg (0.2 mg) / mL))

Package Label-principal Display Panel (40 mg per 200 mL (200 mcg (0.2 mg) / mL))
Milrinone Lactate in 5% Dextrose Injection 40 mg per 200 mL (0.2 mg/mL) in a single-dose flexible container. The label states it is for intravenous infusion only, sterile and preservative-free. Distributed by AuroMedics Pharma LLC, with storage and usage instructions included. NDC 55150-288-10.*
FDA Label Image

Milrinone Lactate Chemical Structure (Milrinone Str)

Milrinone Lactate Chemical Structure (Milrinone Str)
Chemical structure of Milrinone Lactate, showing its molecular framework including a pyridine ring, cyano group, and lactone moiety, associated with the lactate moiety as indicated by additional chemical fragments.*

* 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.