VINORELBINE is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hospira, Inc.. The primary component is Vinorelbine Tartrate.
| Product ID | 61703-341_7133a031-8cfa-4c67-8c09-12711a45184a |
| NDC | 61703-341 |
| Product Type | Human Prescription Drug |
| Proprietary Name | VINORELBINE |
| Generic Name | Vinorelbine |
| Dosage Form | Injection, Solution |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 2007-04-02 |
| Marketing End Date | 2019-05-31 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA076827 |
| Labeler Name | Hospira, Inc. |
| Substance Name | VINORELBINE TARTRATE |
| Active Ingredient Strength | 10 mg/mL |
| Pharm Classes | Vinca Alkaloid [EPC],Vinca Alkaloids [CS] |
| NDC Exclude Flag | N |
| Marketing Start Date | 2007-04-02 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA076827 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2007-04-02 |
| Marketing End Date | 2019-05-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076827 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2007-04-09 |
| Marketing End Date | 2017-10-31 |
| Ingredient | Strength |
|---|---|
| VINORELBINE TARTRATE | 10 mg/mL |
| SPL SET ID: | 06eeaab8-a00d-4b41-b46b-40163f09ecb8 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 25021-204 | Vinorelbine | Vinorelbine |
| 45963-607 | Vinorelbine | Vinorelbine |
| 50742-420 | Vinorelbine | Vinorelbine |
| 50742-427 | Vinorelbine | Vinorelbine |
| 61703-341 | VINORELBINE | vinorelbine |