Home > National Drug Code (NDC) > Vinorelbine

Vinorelbine - 55390-069-01 - (Vinorelbine)

Alphabetical Index


Drug Information of Vinorelbine

Product NDC: 55390-069
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: 55390-069
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076461
Marketing Category: ANDA
Start Marketing Date: 20040211

Package Information of Vinorelbine

Package NDC: 55390-069-01
Package Description: 1 VIAL in 1 BOX, UNIT-DOSE (55390-069-01) > 1 mL in 1 VIAL

NDC Information of Vinorelbine

NDC Code 55390-069-01
Proprietary Name Vinorelbine
Package Description 1 VIAL in 1 BOX, UNIT-DOSE (55390-069-01) > 1 mL in 1 VIAL
Product NDC 55390-069
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Vinorelbine
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20040211
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
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