Docetaxel Anhydrous

Product NDC

69097-371

11-digit product format

690970371

Labeler code

69097

Product ID

69097-371_45fc4959-659e-4b0a-8c0f-7aa2055e7708

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Docetaxel Anhydrous

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Cipla USA Inc.

Application

ANDA209634

Marketing category

ANDA

Marketing start

2018-08-24

Marketing end

0000-00-00

Substance

DOCETAXEL ANHYDROUS

Active strength

80 mg/8mL

Pharmacologic classes

Microtubule Inhibition [PE],Microtubule Inhibitor [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record