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Proleukin
Proleukin - 65483-116-07 - (aldesleukin)
Drug Information of Proleukin
| Product NDC: | 65483-116 |
| Proprietary Name: | Proleukin |
| Non Proprietary Name: | aldesleukin |
| Active Ingredient(s): | 1.1 mg/mL & nbsp; aldesleukin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Proleukin
| Product NDC: | 65483-116 |
| Labeler Name: | Prometheus Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA103293 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19920505 |
Package Information of Proleukin
| Package NDC: | 65483-116-07 |
| Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (65483-116-07) > 1 mL in 1 VIAL, SINGLE-USE |
NDC Information of Proleukin
| NDC Code | 65483-116-07 |
| Proprietary Name | Proleukin |
| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (65483-116-07) > 1 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 65483-116 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | aldesleukin |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19920505 |
| Marketing Category Name | BLA |
| Labeler Name | Prometheus Laboratories Inc. |
| Substance Name | ALDESLEUKIN |
| Strength Number | 1.1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Increased Lymphocyte Activation [PE],Increased Lymphocyte Cell Production [PE],Interleukin-2 [Chemical/Ingredient],Lymphocyte Growth Factor [EPC] |
