HYCAMTIN - 0007-4205-11 - (topotecan hydrochloride)

Alphabetical Index


Drug Information of HYCAMTIN

Product NDC: 0007-4205
Proprietary Name: HYCAMTIN
Non Proprietary Name: topotecan hydrochloride
Active Ingredient(s): .25    mg/1 & nbsp;   topotecan hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of HYCAMTIN

Product NDC: 0007-4205
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020981
Marketing Category: NDA
Start Marketing Date: 20080916

Package Information of HYCAMTIN

Package NDC: 0007-4205-11
Package Description: 10 CAPSULE in 1 BOTTLE (0007-4205-11)

NDC Information of HYCAMTIN

NDC Code 0007-4205-11
Proprietary Name HYCAMTIN
Package Description 10 CAPSULE in 1 BOTTLE (0007-4205-11)
Product NDC 0007-4205
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name topotecan hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20080916
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name TOPOTECAN HYDROCHLORIDE
Strength Number .25
Strength Unit mg/1
Pharmaceutical Classes Topoisomerase Inhibitor [EPC],Topoisomerase Inhibitors [MoA]

Complete Information of HYCAMTIN


General Information