Paclitaxel

Product NDC

51991-936

11-digit product format

519910936

Labeler code

51991

Product ID

51991-936_1fe275b1-bcc3-4644-9314-23dfc3a2f67d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Paclitaxel

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Breckenridge Pharmaceutical, Inc.

Application

ANDA207326

Marketing category

ANDA

Marketing start

2016-09-30

Marketing end

2019-05-31

Substance

PACLITAXEL

Active strength

30 mg/5mL

Pharmacologic classes

Microtubule Inhibition [PE],Microtubule Inhibitor [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record