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Topotecan Hydrochloride - 55390-370-10 - (Topotecan Hydrochloride)

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Drug Information of Topotecan Hydrochloride

Product NDC: 55390-370
Proprietary Name: Topotecan Hydrochloride
Non Proprietary Name: Topotecan Hydrochloride
Active Ingredient(s): 4    mg/4mL & nbsp;   Topotecan Hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Topotecan Hydrochloride

Product NDC: 55390-370
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201191
Marketing Category: ANDA
Start Marketing Date: 20110418

Package Information of Topotecan Hydrochloride

Package NDC: 55390-370-10
Package Description: 1 VIAL in 1 CARTON (55390-370-10) > 4 mL in 1 VIAL

NDC Information of Topotecan Hydrochloride

NDC Code 55390-370-10
Proprietary Name Topotecan Hydrochloride
Package Description 1 VIAL in 1 CARTON (55390-370-10) > 4 mL in 1 VIAL
Product NDC 55390-370
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Topotecan Hydrochloride
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110418
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name TOPOTECAN HYDROCHLORIDE
Strength Number 4
Strength Unit mg/4mL
Pharmaceutical Classes Topoisomerase Inhibitor [EPC],Topoisomerase Inhibitors [MoA]

Complete Information of Topotecan Hydrochloride


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