Product NDC: | 55513-209 |
Proprietary Name: | NEUPOGEN |
Non Proprietary Name: | Filgrastim |
Active Ingredient(s): | 480 ug/.8mL & nbsp; Filgrastim |
Administration Route(s): | INTRAVENOUS; SUBCUTANEOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55513-209 |
Labeler Name: | Amgen Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA103353 |
Marketing Category: | BLA |
Start Marketing Date: | 20001002 |
Package NDC: | 55513-209-10 |
Package Description: | 10 SYRINGE in 1 BOX (55513-209-10) > .8 mL in 1 SYRINGE (55513-209-01) |
NDC Code | 55513-209-10 |
Proprietary Name | NEUPOGEN |
Package Description | 10 SYRINGE in 1 BOX (55513-209-10) > .8 mL in 1 SYRINGE (55513-209-01) |
Product NDC | 55513-209 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Filgrastim |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS; SUBCUTANEOUS |
Start Marketing Date | 20001002 |
Marketing Category Name | BLA |
Labeler Name | Amgen Inc |
Substance Name | FILGRASTIM |
Strength Number | 480 |
Strength Unit | ug/.8mL |
Pharmaceutical Classes | Granulocyte Colony-Stimulating Factor [Chemical/Ingredient],Granulocyte-Macrophage Colony-Stimulating Factor [Chemical/Ingredient],Increased Myeloid Cell Production [PE],Leukocyte Growth Factor [EPC] |