Docetaxel

Product NDC

63739-932

11-digit product format

637390932

Labeler code

63739

Product ID

63739-932_d0cd1191-df76-4b7f-9518-e5f941c347a7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Docetaxel

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

McKesson Packaging Services a business unit of McKesson Corporation

Application

NDA201195

Marketing category

NDA

Marketing start

2013-05-15

Marketing end

0000-00-00

Substance

DOCETAXEL ANHYDROUS

Active strength

20 mg/mL

Pharmacologic classes

Microtubule Inhibition [PE],Microtubule Inhibitor [EPC]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record