Home > National Drug Code (NDC) > Vinorelbine

Vinorelbine - 0069-0205-10 - (Vinorelbine)

Alphabetical Index


Drug Information of Vinorelbine

Product NDC: 0069-0205
Proprietary Name: Vinorelbine
Non Proprietary Name: Vinorelbine
Active Ingredient(s): 10    mg/mL & nbsp;   Vinorelbine
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Vinorelbine

Product NDC: 0069-0205
Labeler Name: Pfizer Laboratories Div Pfizer Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200148
Marketing Category: ANDA
Start Marketing Date: 20120901

Package Information of Vinorelbine

Package NDC: 0069-0205-10
Package Description: 1 mL in 1 VIAL (0069-0205-10)

NDC Information of Vinorelbine

NDC Code 0069-0205-10
Proprietary Name Vinorelbine
Package Description 1 mL in 1 VIAL (0069-0205-10)
Product NDC 0069-0205
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Vinorelbine
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120901
Marketing Category Name ANDA
Labeler Name Pfizer Laboratories Div Pfizer 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


General Information