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Topotecan
Topotecan - 0409-0302-01 - (TOPOTECAN HYDROCHLORIDE)
Drug Information of Topotecan
| Product NDC: | 0409-0302 |
| Proprietary Name: | Topotecan |
| Non Proprietary Name: | TOPOTECAN HYDROCHLORIDE |
| Active Ingredient(s): | 1 mg/mL & nbsp; TOPOTECAN HYDROCHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Topotecan
| Product NDC: | 0409-0302 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA200582 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110202 |
Package Information of Topotecan
| Package NDC: | 0409-0302-01 |
| Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (0409-0302-01) > 4 mL in 1 VIAL, SINGLE-USE |
NDC Information of Topotecan
| NDC Code | 0409-0302-01 |
| Proprietary Name | Topotecan |
| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (0409-0302-01) > 4 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 0409-0302 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | TOPOTECAN HYDROCHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110202 |
| Marketing Category Name | NDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | TOPOTECAN HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Topoisomerase Inhibitor [EPC],Topoisomerase Inhibitors [MoA] |
