Topotecan is a Intravenous Injection, Solution, Concentrate in the Human Prescription Drug category. It is labeled and distributed by Teva Parenteral Medicines, Inc.. The primary component is Topotecan Hydrochloride.
Product ID | 0703-4714_ae304685-a4f5-43fe-8ea1-84ccd123b5c5 |
NDC | 0703-4714 |
Product Type | Human Prescription Drug |
Proprietary Name | Topotecan |
Generic Name | Topotecan |
Dosage Form | Injection, Solution, Concentrate |
Route of Administration | INTRAVENOUS |
Marketing Start Date | 2013-05-21 |
Marketing Category | NDA / NDA |
Application Number | NDA022453 |
Labeler Name | Teva Parenteral Medicines, Inc. |
Substance Name | TOPOTECAN HYDROCHLORIDE |
Active Ingredient Strength | 1 mg/mL |
Pharm Classes | Topoisomerase Inhibitor [EPC],Topoisomerase Inhibitors [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2013-05-21 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA022453 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2013-05-21 |
Marketing Category | NDA |
Application Number | NDA022453 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2013-05-21 |
Ingredient | Strength |
---|---|
TOPOTECAN HYDROCHLORIDE | 1 mg/mL |
SPL SET ID: | 9683e3be-7d23-4ba7-9fe9-9762963604f0 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0409-0302 | Topotecan | TOPOTECAN |
0703-4714 | Topotecan | Topotecan |
16729-243 | Topotecan | Topotecan |
25021-236 | topotecan | topotecan |
50742-404 | Topotecan | Topotecan |
66758-051 | Topotecan | Topotecan |
67457-662 | TOPOTECAN | TOPOTECAN |
71288-127 | Topotecan | Topotecan Hydrochloride |
0078-0672 | HYCAMTIN | topotecan |
0078-0673 | HYCAMTIN | topotecan |