Doxorubicin Hydrochloride liposome

Product NDC

59676-966

11-digit product format

596760966

Labeler code

59676

Product ID

59676-966_2100bf6a-67f3-11e9-9dee-13020199106d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

doxorubicin hydrochloride

Dosage form

INJECTION, SUSPENSION, LIPOSOMAL

Route

INTRAVENOUS

Labeler

Janssen Products, LP

Application

NDA050718

Marketing category

NDA

Marketing start

2017-06-26

Marketing end

2020-10-31

Substance

DOXORUBICIN HYDROCHLORIDE

Active strength

2 mg/mL

Pharmacologic classes

Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [CS],Topoisomerase Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record