Pulmotech Maa Injection, Powder, Lyophilized, For Suspension
Product Images NDC 69945-139

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pulmotech Maa (NDC 69945-139). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Curium 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

Pulmotech Maa 1

FDA Label Image

Pulmotech Maa 2

Pulmotech Maa 2
This is a description of a kit for the preparation of technetium Tc 99m albumin aggregated injection. The kit is meant for intravenous and intraperitoneal use. It includes 30 multiple-dose vials of Pumotech MAAvis and each vial contains 2mg Abumin Aggregated, 71mg Al Human, 022mo maximum stannous chloride, and 01mg of tannous chloride. Before radiolabeling, there is a required SO radioassay formation abels st I G T Prescribing formatin. After radiolabeling, the vials need to be stored shielded in the refrigerator at 2 to 8°C (36"t 46°F) and used within 18 hours. The description suggests that the kit is used in the medical or healthcare industry for imaging procedures.*
FDA Label Image

Pulmotech Maa 3

Pulmotech Maa 3
The text is a product description of a kit for the preparation of a radiolabeled injection used for intravenous and intraperitoneal use. It contains albumin human, stannous chloride, and sodium chloride. The kit should be stored at 2° to 25°C before radiolabeling and in the refrigerator after radiolabeling. The dosage should be obtained from the prescribing information. The product is manufactured by Curium 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.