Docetaxel - 16729-231-64 - (Docetaxel)

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Drug Information of Docetaxel

Product NDC: 16729-231
Proprietary Name: Docetaxel
Non Proprietary Name: Docetaxel
Active Ingredient(s): 20    mg/mL & nbsp;   Docetaxel
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Docetaxel

Product NDC: 16729-231
Labeler Name: Accord Healthcare Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA201195
Marketing Category: NDA
Start Marketing Date: 20120701

Package Information of Docetaxel

Package NDC: 16729-231-64
Package Description: 1 VIAL, SINGLE-USE in 1 CARTON (16729-231-64) > 4 mL in 1 VIAL, SINGLE-USE

NDC Information of Docetaxel

NDC Code 16729-231-64
Proprietary Name Docetaxel
Package Description 1 VIAL, SINGLE-USE in 1 CARTON (16729-231-64) > 4 mL in 1 VIAL, SINGLE-USE
Product NDC 16729-231
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Docetaxel
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120701
Marketing Category Name NDA
Labeler Name Accord Healthcare Inc.
Substance Name DOCETAXEL
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Microtubule Inhibition [PE],Microtubule Inhibitor [EPC]

Complete Information of Docetaxel


General Information