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Vinblastine Sulfate - 55390-091-10 - (Vinblastine Sulfate)

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Drug Information of Vinblastine Sulfate

Product NDC: 55390-091
Proprietary Name: Vinblastine Sulfate
Non Proprietary Name: Vinblastine Sulfate
Active Ingredient(s): 10    mg/10mL & nbsp;   Vinblastine Sulfate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Vinblastine Sulfate

Product NDC: 55390-091
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089395
Marketing Category: ANDA
Start Marketing Date: 19960501

Package Information of Vinblastine Sulfate

Package NDC: 55390-091-10
Package Description: 10 VIAL in 1 BOX (55390-091-10) > 10 mL in 1 VIAL

NDC Information of Vinblastine Sulfate

NDC Code 55390-091-10
Proprietary Name Vinblastine Sulfate
Package Description 10 VIAL in 1 BOX (55390-091-10) > 10 mL in 1 VIAL
Product NDC 55390-091
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Vinblastine Sulfate
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19960501
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name VINBLASTINE SULFATE
Strength Number 10
Strength Unit mg/10mL
Pharmaceutical Classes Vinca Alkaloid [EPC],Vinca Alkaloids [Chemical/Ingredient]

Complete Information of Vinblastine Sulfate


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