Albutein Injection, Solution
Product Images NDC 68516-5216

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Albutein (NDC 68516-5216). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Grifols Usa, 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

68516 5216 0 Carton

The packaging label for ALBUTEIN FlexBag 25% features Albumin (Human) U.S.P. in a 25 g per 100 mL solution. The label states 5 x 100 mL single-dose containers and highlights storage instructions to keep below 30°C and avoid freezing. The labeler is GRIFOLS USA, LLC. The product NDC is 68516-5216-0. The design uses blue, white, and red colors with distinct branding and includes barcode and lot/expiration placeholders.*

FDA Label Image

68516-5216-8-bag (68516 5216 8 Bag)

ALBUTEIN FlexBag 25% Albumin (Human) injection solution labeled with 25 g per 100 mL strength. The label states it is for intravenous use, single-dose, Rx only. It includes manufacturer information for Grifols Biologicals LLC, Los Angeles, CA, and instructions for storage and handling, including heat treatment and storage temperature. The label also displays a barcode and QR code on the flexible infusion bag.*

FDA Label Image

Figures 1,2,3,4 (Fig 1 2 3 4)

An instructional diagram illustrating four steps for preparing an intravenous solution bag: Figure 1 shows hands removing a protective cap; Figure 2 depicts opening a port or spout; Figure 3 shows holding a tap or valve below the bag; and Figure 4 illustrates connecting a syringe to the bag's port for withdrawal or injection.*

* 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.