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Aloxi
Aloxi - 62856-798-01 - (palonosetron hydrochloride)
Drug Information of Aloxi
| Product NDC: | 62856-798 |
| Proprietary Name: | Aloxi |
| Non Proprietary Name: | palonosetron hydrochloride |
| Active Ingredient(s): | .075 mg/1.5mL & nbsp; palonosetron hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aloxi
| Product NDC: | 62856-798 |
| Labeler Name: | Eisai, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021372 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080229 |
Package Information of Aloxi
| Package NDC: | 62856-798-01 |
| Package Description: | 5 VIAL in 1 CARTON (62856-798-01) > 1.5 mL in 1 VIAL |
NDC Information of Aloxi
| NDC Code | 62856-798-01 |
| Proprietary Name | Aloxi |
| Package Description | 5 VIAL in 1 CARTON (62856-798-01) > 1.5 mL in 1 VIAL |
| Product NDC | 62856-798 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | palonosetron hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20080229 |
| Marketing Category Name | NDA |
| Labeler Name | Eisai, Inc |
| Substance Name | PALONOSETRON HYDROCHLORIDE |
| Strength Number | .075 |
| Strength Unit | mg/1.5mL |
| Pharmaceutical Classes | Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC] |
