Daunorubicin Hydrochloride Injection
Product Images NDC 0143-9551

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Daunorubicin Hydrochloride (NDC 0143-9551). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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

Structural Formula (Daunorubicin Hydrochloride 1)

Chemical structure of Daunorubicin Hydrochloride, illustrating its molecular framework including rings, hydroxyl groups, methoxy groups, and hydrochloride component.*

FDA Label Image

Daunorubicin HCl Injection Vial Label 20 mg/4ml (Daunorubicin Hydrochloride 2)

Daunorubicin Hydrochloride Injection 20 mg/4 mL (5 mg/mL) single dose vial label for intravenous use only. The label includes storage instructions, active ingredient concentration, and distributor information, Hikma Pharmaceuticals USA Inc.*

FDA Label Image

Daunorubicin HCl Injection Vial Label 50 mg/10 mL (Daunorubicin Hydrochloride 3)

Daunorubicin Hydrochloride Injection 5 mg/mL (50 mg/10 mL) single-dose vial label for intravenous use, by Hikma Pharmaceuticals USA Inc. The label includes dosing details and storage instructions, emphasizing protection from light and refrigeration storage between 2° to 8°C (36° to 46°F). Manufactured by THYMOORGAN PHARMAZIE GmbH, Germany, and distributed by West-Ward in Eatontown, NJ.*

FDA Label Image

Representative Carton Serialization Image (Daunorubicin Hydrochloride 4)

Daunorubicin Hydrochloride 5 mg/mL injection label for intravenous use by Hikma Pharmaceuticals USA Inc. The label includes a QR code and text fields for GTIN, serial number, expiration date, and lot number.*

* 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.