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Topotecan Hydrochloride - 66435-410-05 - (topotecan hydrochloride)

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Drug Information of Topotecan Hydrochloride

Product NDC: 66435-410
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, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Topotecan Hydrochloride

Product NDC: 66435-410
Labeler Name: Three Rivers Pharmaceuticals, LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091199
Marketing Category: ANDA
Start Marketing Date: 20101202

Package Information of Topotecan Hydrochloride

Package NDC: 66435-410-05
Package Description: 5 VIAL, GLASS in 1 CARTON (66435-410-05) > 4 mL in 1 VIAL, GLASS

NDC Information of Topotecan Hydrochloride

NDC Code 66435-410-05
Proprietary Name Topotecan Hydrochloride
Package Description 5 VIAL, GLASS in 1 CARTON (66435-410-05) > 4 mL in 1 VIAL, GLASS
Product NDC 66435-410
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name topotecan hydrochloride
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20101202
Marketing Category Name ANDA
Labeler Name Three Rivers Pharmaceuticals, LLC.
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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