NDC Code |
55513-221-01 |
Proprietary Name |
Nplate |
Package Description |
1 VIAL in 1 CARTON (55513-221-01) > .5 mL in 1 VIAL |
Product NDC |
55513-221 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
romiplostim |
Dosage Form Name |
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Route Name |
SUBCUTANEOUS |
Start Marketing Date |
20080825 |
Marketing Category Name |
BLA |
Labeler Name |
Amgen Inc |
Substance Name |
ROMIPLOSTIM |
Strength Number |
250 |
Strength Unit |
ug/.5mL |
Pharmaceutical Classes |
Increased Megakaryocyte Maturation [PE],Increased Platelet Production [PE],Thrombopoiesis Stimulating Agent [EPC],Thrombopoietin Receptor Agonists [MoA],Thrombopoietin Receptor Interactions [MoA] |