Structural Formula (Image 01)
Doxil Injection, Suspension, Liposomal
Product Images NDC 0338-0063
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Doxil (NDC 0338-0063). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Baxter Healthcare Company, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
Mpeg-dspe Structural Formula (Image 02)
Hspc Structural Formula (Image 03)
Representation Of A Stealth Liposome (Image 04)
Figure 1 (Image 05)
This appears to be a statistical report and includes some kind of medical intervention. There are mentions of a treatment called Bortezomib and a p-value of less than
Representative 20 mg Container Label (Image 06)
This is a description of a medication with the NDC code 0338-0063-01. It is a liposome injection for intravenous infusion, with 20 mg in 10 mL (2 mg/mL) dosage. It is a single-dose vial and the unused portion should be discarded. This medication is a LIPOSOMAL FORMULATION, and it is important not to substitute it for doxorubicin Hydrochloride. It is to be used under prescription only and is cytotoxic. It should be refrigerated between 36°-46°F, but not frozen. Dosage information can be found in the package insert. It is manufactured by Baxter Healthcare Corporation located in Deerfield, IL 60015.*
Representative Carton Label 0338-0063-01 (Image 07)
Representative Carton Label 20 mg Taiwan (Image 08)
Representative Container Label 50 mg (Image 09)
DOXIL is a liposomal formulation of DOXOrubicin Hydrochloride injection used for intravenous infusion only. Each 10mL vial contains 20mg of DOXOrubicin Hydrochloride. It should not be substituted for other DOXOrubicin Hydrochloride products. The drug should be refrigerated at 2.5°C and should not be frozen. The liposomes used in DOXIL carries doxorubicin hydrochloride and are composed of cholesterol, ycropensted s0y phosphathholin 15, Necrbonyle methanypolyetyien and others. The concentration of doxorubicin hydrochloride in the injection is approximately 2mg/mL. The drug is only available in a 10mL vial and should be administered by a licensed healthcare provider.*
Representative Carton Label 0338-0067-01 (Image 10)
This is a medication with the National Drug Code (NDC) 0338-0067-01. It needs to be refrigerated between 2°-8°C (36°46°P) and should be discarded if not used completely. It contains a liposomal formulation of 50mg in 25 mL of Doxorubicin Hydrochloride, which is used for intravenous infusion only as a cytotoxic. The text includes a warning not to substitute it for regular Doxorubicin. There is also a reference to a package insert for dosage information.*
Representative Carton Label 50 mg Taiwan (Image 11)
This text appears to be a combination of a medical prescription and a packaging label for a drug called DOXIL, which is a liposome injection. The label indicates that the drug should be diluted with 5% Dextrose Inecton, USP and discarded if unused. It also warns against substituting DOXIL with DOXORUBICIN Hydrochloride and recommends storage between 2-8°C and not to freeze. However, there is no information about the correct use, indications, or side effects of this medication.*
Image 12
DOXIL is a liposome injection containing doxorubicin Hycrochloride, used for the treatment of ovarian and breast cancer. The liposome carriers provide increased effectiveness and reduce side effects. It is essential not to use DOXIL as a substitute for DOXORUBICIN Hydrochloride. The drug is manufactured and marketed by Baxter Healthcare in Deerfield, IL. The injection has a unique composition and should only be used as directed by a physician.*
Image 13
* 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.
