Docetaxel - 66758-050-03 - (docetaxel)

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Drug Information of Docetaxel

Product NDC: 66758-050
Proprietary Name: Docetaxel
Non Proprietary Name: docetaxel
Active Ingredient(s): 10    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: 66758-050
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA201525
Marketing Category: NDA
Start Marketing Date: 20110629

Package Information of Docetaxel

Package NDC: 66758-050-03
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (66758-050-03) > 16 mL in 1 VIAL, MULTI-DOSE

NDC Information of Docetaxel

NDC Code 66758-050-03
Proprietary Name Docetaxel
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (66758-050-03) > 16 mL in 1 VIAL, MULTI-DOSE
Product NDC 66758-050
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name docetaxel
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110629
Marketing Category Name NDA
Labeler Name Sandoz Inc
Substance Name DOCETAXEL
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Docetaxel


General Information