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Fusilev
Fusilev - 68152-101-00 - (levoleucovorin)
Drug Information of Fusilev
| Product NDC: | 68152-101 |
| Proprietary Name: | Fusilev |
| Non Proprietary Name: | levoleucovorin |
| Active Ingredient(s): | 50 mg/5mL & nbsp; levoleucovorin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fusilev
| Product NDC: | 68152-101 |
| Labeler Name: | Spectrum Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020140 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080815 |
Package Information of Fusilev
| Package NDC: | 68152-101-00 |
| Package Description: | 1 VIAL in 1 CARTON (68152-101-00) > 5 mL in 1 VIAL |
NDC Information of Fusilev
| NDC Code | 68152-101-00 |
| Proprietary Name | Fusilev |
| Package Description | 1 VIAL in 1 CARTON (68152-101-00) > 5 mL in 1 VIAL |
| Product NDC | 68152-101 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levoleucovorin |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20080815 |
| Marketing Category Name | NDA |
| Labeler Name | Spectrum Pharmaceuticals, Inc. |
| Substance Name | LEVOLEUCOVORIN CALCIUM |
| Strength Number | 50 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
