Paclitaxel - 63323-763-16 - (PACLITAXEL)

Alphabetical Index


Drug Information of Paclitaxel

Product NDC: 63323-763
Proprietary Name: Paclitaxel
Non Proprietary Name: PACLITAXEL
Active Ingredient(s): 6    mg/mL & nbsp;   PACLITAXEL
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Paclitaxel

Product NDC: 63323-763
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077574
Marketing Category: ANDA
Start Marketing Date: 20090320

Package Information of Paclitaxel

Package NDC: 63323-763-16
Package Description: 1 VIAL in 1 BOX (63323-763-16) > 16.7 mL in 1 VIAL

NDC Information of Paclitaxel

NDC Code 63323-763-16
Proprietary Name Paclitaxel
Package Description 1 VIAL in 1 BOX (63323-763-16) > 16.7 mL in 1 VIAL
Product NDC 63323-763
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PACLITAXEL
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20090320
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name PACLITAXEL
Strength Number 6
Strength Unit mg/mL
Pharmaceutical Classes Microtubule Inhibition [PE],Microtubule Inhibitor [EPC]

Complete Information of Paclitaxel


General Information