Docetaxel - 0955-1020-01 - (Docetaxel)

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Drug Information of Docetaxel

Product NDC: 0955-1020
Proprietary Name: Docetaxel
Non Proprietary Name: Docetaxel
Active Ingredient(s): 20    mg/mL & nbsp;   Docetaxel
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION, CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of Docetaxel

Product NDC: 0955-1020
Labeler Name: Winthrop U.S.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020449
Marketing Category: NDA
Start Marketing Date: 20101021

Package Information of Docetaxel

Package NDC: 0955-1020-01
Package Description: 1 VIAL, GLASS in 1 CARTON (0955-1020-01) > 1 mL in 1 VIAL, GLASS

NDC Information of Docetaxel

NDC Code 0955-1020-01
Proprietary Name Docetaxel
Package Description 1 VIAL, GLASS in 1 CARTON (0955-1020-01) > 1 mL in 1 VIAL, GLASS
Product NDC 0955-1020
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Docetaxel
Dosage Form Name INJECTION, SOLUTION, CONCENTRATE
Route Name INTRAVENOUS
Start Marketing Date 20101021
Marketing Category Name NDA
Labeler Name Winthrop U.S.
Substance Name DOCETAXEL
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Microtubule Inhibition [PE],Microtubule Inhibitor [EPC]

Complete Information of Docetaxel


General Information