Flexbumin Solution
Product Images NDC 0944-0493

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Flexbumin (NDC 0944-0493). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Takeda Pharmaceuticals America, 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

Bag Label (Flexbumin 01)

Label for FLEXBUMIN 25% USP Albumin (Human) solution for infusion, 50 mL single-dose container. The label includes product details such as albumin content from venous plasma, storage instructions, cautions, NDC 0944-0493-03, code 2G0201, and manufacturer Takeda Pharmaceuticals America, Inc. The Takeda logo and a barcode are also visible.*

FDA Label Image

Intermediate Label (Flexbumin 02)

Label for FLEXBUMIN 25% USP/50 ml solution for infusion, Albumin Human, single-dose containers. The label includes the barcode, NDC 0944-0493-01, and manufacturer Takeda Pharmaceuticals America, Inc. Storage instructions advise keeping at room temperature, not to exceed 25°C, and protecting from freezing. Warnings mention administering within 4 hours and specific cautions for use.*

FDA Label Image

Bag Label 100 mL (Flexbumin 03)

FLEXBUMIN 25% USP/100mL solution for infusion, Albumin (Human), single-dose intravenous solution. The label shows a 100 mL container, manufactured by Takeda Pharmaceuticals America, Inc., with product NDC 0944-0493. The label includes storage instructions, cautions, and a barcode.*

FDA Label Image

Intermediate Label 100 mL (Flexbumin 04)

Label for FLEXBUMIN 25% USP per 100 mL solution for infusion, containing Albumin (Human). The packaging indicates single-dose containers, 6 x 100 mL, from Takeda Pharmaceuticals America, Inc. The label includes usage cautions, storage recommendations, NDC 0944-0493-02, and a barcode.*

* 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.