Busulfex
Product Images NDC 59148-070

3 FDA label images from Otsuka America Pharmaceutical, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Busulfex (NDC 59148-070). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Otsuka America Pharmaceutical, 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

Chemical Structure (Busulfex 01)

Chemical Structure (Busulfex 01)
Chemical structure of busulfan, illustrated as a molecular formula showing the arrangement of atoms including methyl groups, sulfonyl groups, and a butane linker.*
FDA Label Image

Principal Display Panel (10 mL Vial Carton)

Principal Display Panel (10 mL Vial Carton)
Label for Busulfex (busulfan) Injection 60 mg/10 mL (6 mg/mL), a sterile single-dose vial for intravenous infusion. The 10 mL vial contains 60 mg busulfan, 3.3 mL dimethylacetamide, and 6.7 mL polyethylene glycol-400. It is distributed by Otsuka America Pharmaceutical, Inc., Rockville, MD. The label includes storage instructions and cautions about dilution before use.*
FDA Label Image

Principal Display Panel (Eight 10 mL Vials Carton)

Principal Display Panel (Eight 10 mL Vials Carton)
BUSULFEX (busulfan) Injection 60 mg/10 mL (6 mg/mL) 10 mL single-dose vial packaging label. Distributed and marketed by Otsuka America Pharmaceutical, Inc., and manufactured by Baxter Oncology GmbH. The label includes dosage form, strength, vial volume, and storage instructions, indicating it is for intravenous infusion only and must be diluted before use.*

* 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.