Obizur Kit
Product Images NDC 0944-5001

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Obizur (NDC 0944-5001). 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

Figure A (Obizur 01)

FDA Label Image

Figure B (Obizur 02)

FDA Label Image

Figure C (Obizur 03)

FDA Label Image

Figure D (Obizur 04)

FDA Label Image

Figure E (Obizur 05)

FDA Label Image

Figure F (Obizur 06)

FDA Label Image

Figure G (Obizur 07)

FDA Label Image

Figure H (Obizur 08)

FDA Label Image

Figure I (Obizur 09)

FDA Label Image

Principal Display Panel (Kit Carton)

Principal Display Panel (Kit Carton)
This is a description of OBIZUR, a recombinant antihemophilic factor made from porcine sequence. It comes in a single-dose vial as a lyophilized powder for intravenous administration after reconstitution. The product contains no preservative and is sterile and nonpyrogenic. It should be stored at a temperature between 2°C to 8°C and not beyond the expiration date. The package includes a vial adapter, diluent, and a package insert that provides dosage and administration information. The product is not made with natural rubber latex.*

* 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.