Daunorubicin Hydrochloride Injection, Solution
Product Images NDC 71288-182

View Photos of 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 Daunorubicin Hydrochloride (NDC 71288-182). 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

Principal Display Panel (DAUNOrubicin Hydrochloride Injection 20 mg per 4 mL Carton)

Principal Display Panel (DAUNOrubicin Hydrochloride Injection 20 mg per 4 mL Carton)
Packaging label for DAUNOrubicin Hydrochloride Injection 20 mg per 4 mL (5 mg per mL) from Meitheal Pharmaceuticals Inc. The label states that this is for intravenous use only, includes a caution that the product is a cytotoxic agent, and indicates it contains 10 single-dose vials of 4 mL each. Additional label text includes storage instructions and manufacturer details.*
FDA Label Image

Structural Formula (Daunorubicin Structure)

Structural Formula (Daunorubicin Structure)
Chemical structure diagram of daunorubicin hydrochloride, showing the molecular arrangement including rings, hydroxyl groups, and hydrochloride component.*
FDA Label Image

Principal Display Panel (DAUNOrubicin Hydrochloride Injection 20 mg per 4 mL Container Label)

Principal Display Panel (DAUNOrubicin Hydrochloride Injection 20 mg per 4 mL Container Label)
Label for daunorubicin hydrochloride injection 20 mg per 4 mL (5 mg per mL) in a 4 mL single-dose vial by Meitheal Pharmaceuticals Inc. The label states it is for intravenous use only, includes the NDC 71288-182-04, and provides dosage form and storage instructions.*

* 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.