Product NDC: | 0024-5844 |
Proprietary Name: | Leukine |
Non Proprietary Name: | SARGRAMOSTIM |
Active Ingredient(s): | 500 ug/mL & nbsp; SARGRAMOSTIM |
Administration Route(s): | INTRAVENOUS; SUBCUTANEOUS |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0024-5844 |
Labeler Name: | sanofi-aventis U.S. LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA103362 |
Marketing Category: | BLA |
Start Marketing Date: | 19961201 |
Package NDC: | 0024-5844-05 |
Package Description: | 5 VIAL in 1 CARTON (0024-5844-05) > 1 mL in 1 VIAL |
NDC Code | 0024-5844-05 |
Proprietary Name | Leukine |
Package Description | 5 VIAL in 1 CARTON (0024-5844-05) > 1 mL in 1 VIAL |
Product NDC | 0024-5844 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | SARGRAMOSTIM |
Dosage Form Name | LIQUID |
Route Name | INTRAVENOUS; SUBCUTANEOUS |
Start Marketing Date | 19961201 |
Marketing Category Name | BLA |
Labeler Name | sanofi-aventis U.S. LLC |
Substance Name | SARGRAMOSTIM |
Strength Number | 500 |
Strength Unit | ug/mL |
Pharmaceutical Classes | Granulocyte Colony-Stimulating Factor [Chemical/Ingredient],Granulocyte-Macrophage Colony-Stimulating Factor [Chemical/Ingredient],Increased Myeloid Cell Production [PE],Leukocyte Growth Factor [EPC] |