Etoposide - 55390-293-01 - (Etoposide)

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Drug Information of Etoposide

Product NDC: 55390-293
Proprietary Name: Etoposide
Non Proprietary Name: Etoposide
Active Ingredient(s): 20    mg/mL & nbsp;   Etoposide
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Etoposide

Product NDC: 55390-293
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074290
Marketing Category: ANDA
Start Marketing Date: 19970201

Package Information of Etoposide

Package NDC: 55390-293-01
Package Description: 1 VIAL in 1 BOX, UNIT-DOSE (55390-293-01) > 50 mL in 1 VIAL

NDC Information of Etoposide

NDC Code 55390-293-01
Proprietary Name Etoposide
Package Description 1 VIAL in 1 BOX, UNIT-DOSE (55390-293-01) > 50 mL in 1 VIAL
Product NDC 55390-293
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Etoposide
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 19970201
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name ETOPOSIDE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Topoisomerase Inhibitor [EPC],Topoisomerase Inhibitors [MoA]

Complete Information of Etoposide


General Information