Docetaxel - 0409-0201-20 - (DOCETAXEL ANHYDROUS)

Alphabetical Index


Drug Information of Docetaxel

Product NDC: 0409-0201
Proprietary Name: Docetaxel
Non Proprietary Name: DOCETAXEL ANHYDROUS
Active Ingredient(s): 10    mg/mL & nbsp;   DOCETAXEL ANHYDROUS
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Docetaxel

Product NDC: 0409-0201
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022234
Marketing Category: NDA
Start Marketing Date: 20110308

Package Information of Docetaxel

Package NDC: 0409-0201-20
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (0409-0201-20) > 16 mL in 1 VIAL, MULTI-DOSE

NDC Information of Docetaxel

NDC Code 0409-0201-20
Proprietary Name Docetaxel
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (0409-0201-20) > 16 mL in 1 VIAL, MULTI-DOSE
Product NDC 0409-0201
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DOCETAXEL ANHYDROUS
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110308
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name DOCETAXEL ANHYDROUS
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Microtubule Inhibition [PE],Microtubule Inhibitor [EPC]

Complete Information of Docetaxel


General Information