Paclitaxel - 47351-009-50 - (Paclitaxel)

Alphabetical Index


Drug Information of Paclitaxel

Product NDC: 47351-009
Proprietary Name: Paclitaxel
Non Proprietary Name: Paclitaxel
Active Ingredient(s): 6    mg/mL & nbsp;   Paclitaxel
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Paclitaxel

Product NDC: 47351-009
Labeler Name: Onco Therapies Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091540
Marketing Category: ANDA
Start Marketing Date: 20110930

Package Information of Paclitaxel

Package NDC: 47351-009-50
Package Description: 50 mL in 1 VIAL (47351-009-50)

NDC Information of Paclitaxel

NDC Code 47351-009-50
Proprietary Name Paclitaxel
Package Description 50 mL in 1 VIAL (47351-009-50)
Product NDC 47351-009
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paclitaxel
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20110930
Marketing Category Name ANDA
Labeler Name Onco Therapies Limited
Substance Name PACLITAXEL
Strength Number 6
Strength Unit mg/mL
Pharmaceutical Classes Microtubule Inhibition [PE],Microtubule Inhibitor [EPC]

Complete Information of Paclitaxel


General Information