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Vinorelbine Tartrate - 61703-341-09 - (VINORELBINE TARTRATE)

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Drug Information of Vinorelbine Tartrate

Product NDC: 61703-341
Proprietary Name: Vinorelbine Tartrate
Non Proprietary Name: VINORELBINE TARTRATE
Active Ingredient(s): 10    mg/mL & nbsp;   VINORELBINE TARTRATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Vinorelbine Tartrate

Product NDC: 61703-341
Labeler Name: Hospira Worldwide, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076827
Marketing Category: ANDA
Start Marketing Date: 20050602

Package Information of Vinorelbine Tartrate

Package NDC: 61703-341-09
Package Description: 1 VIAL, SINGLE-USE in 1 CARTON (61703-341-09) > 5 mL in 1 VIAL, SINGLE-USE

NDC Information of Vinorelbine Tartrate

NDC Code 61703-341-09
Proprietary Name Vinorelbine Tartrate
Package Description 1 VIAL, SINGLE-USE in 1 CARTON (61703-341-09) > 5 mL in 1 VIAL, SINGLE-USE
Product NDC 61703-341
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name VINORELBINE TARTRATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20050602
Marketing Category Name ANDA
Labeler Name Hospira Worldwide, Inc.
Substance Name VINORELBINE TARTRATE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Vinca Alkaloid [EPC],Vinca Alkaloids [Chemical/Ingredient]

Complete Information of Vinorelbine Tartrate


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