Docetaxel

Product NDC

39822-2120

11-digit product format

398222120

Labeler code

39822

Product ID

39822-2120_f66ad73d-5c3e-4bc2-ac1b-0aafd155876d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

docetaxel

Dosage form

INJECTION, SOLUTION, CONCENTRATE

Route

INTRAVENOUS

Labeler

X-GEN Pharmaceuticals, Inc.

Application

ANDA206177

Marketing category

ANDA

Marketing start

2017-04-17

Marketing end

0000-00-00

Substance

DOCETAXEL

Active strength

20 mg/mL

Pharmacologic classes

Microtubule Inhibition [PE],Microtubule Inhibitor [EPC]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record