DOCEFREZ - 47335-286-41 - (docetaxel anhydrous)

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Drug Information of DOCEFREZ

Product NDC: 47335-286
Proprietary Name: DOCEFREZ
Non Proprietary Name: docetaxel anhydrous
Active Ingredient(s):    & nbsp;   docetaxel anhydrous
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of DOCEFREZ

Product NDC: 47335-286
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022534
Marketing Category: NDA
Start Marketing Date: 20110503

Package Information of DOCEFREZ

Package NDC: 47335-286-41
Package Description: 1 KIT in 1 CARTON (47335-286-41) * 1 mL in 1 VIAL, SINGLE-USE * 4.21 mL in 1 VIAL, SINGLE-USE (47335-288-40)

NDC Information of DOCEFREZ

NDC Code 47335-286-41
Proprietary Name DOCEFREZ
Package Description 1 KIT in 1 CARTON (47335-286-41) * 1 mL in 1 VIAL, SINGLE-USE * 4.21 mL in 1 VIAL, SINGLE-USE (47335-288-40)
Product NDC 47335-286
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name docetaxel anhydrous
Dosage Form Name KIT
Route Name
Start Marketing Date 20110503
Marketing Category Name NDA
Labeler Name Sun Pharma Global FZE
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of DOCEFREZ


General Information