Product NDC: | 66758-051 |
Proprietary Name: | Topotecan |
Non Proprietary Name: | Topotecan |
Active Ingredient(s): | 1 mg/mL & nbsp; Topotecan |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66758-051 |
Labeler Name: | Sandoz Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA200199 |
Marketing Category: | NDA |
Start Marketing Date: | 20110225 |
Package NDC: | 66758-051-03 |
Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (66758-051-03) > 3 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 66758-051-03 |
Proprietary Name | Topotecan |
Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (66758-051-03) > 3 mL in 1 VIAL, MULTI-DOSE |
Product NDC | 66758-051 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Topotecan |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20110225 |
Marketing Category Name | NDA |
Labeler Name | Sandoz Inc |
Substance Name | TOPOTECAN HYDROCHLORIDE |
Strength Number | 1 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Topoisomerase Inhibitor [EPC],Topoisomerase Inhibitors [MoA] |