Busulfan Injection, Solution
Product Images NDC 71288-158

3 FDA label images from Meitheal Pharmaceuticals 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 Busulfan (NDC 71288-158). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meitheal Pharmaceuticals 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 (Bus08 0000 01)

Figure (Bus08 0000 01)
Chemical structure diagram of busulfan showing the molecular arrangement of its atoms and bonds in a two-dimensional format.*
FDA Label Image

Principal Display Panel (Busulfan Injection 60 mg Vial Label)

Principal Display Panel (Busulfan Injection 60 mg Vial Label)
Busulfan Injection label for intravenous infusion, 60 mg per 10 mL (6 mg/mL) single-dose vial by Meitheal Pharmaceuticals Inc. The preservative-free solution is cytotoxic and must be diluted before use. The label includes storage instructions and cautions, showing NDC 71288-158-95 and barcode details.*
FDA Label Image

Principal Display Panel (Busulfan Injection 60 mg Carton)

Principal Display Panel (Busulfan Injection 60 mg Carton)
Busulfan Injection 60 mg per 10 mL (6 mg per mL) intravenous solution packaging label from Meitheal Pharmaceuticals Inc. It contains 8 x 10 mL single-dose vials. The label highlights that the product is a cytotoxic agent, sterile, preservative-free, and must be diluted before use. Storage instructions indicate refrigeration between 2° to 8°C. The label bears the Novaplus brand and includes a barcode and QR code for prescription purposes.*

* 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.