55513-221 : Nplate 250 ug/.5ml Subcutaneous Injection, Powder, Lyophilized, for Solution


NDC: 55513-221
Labeler: Amgen Inc
Product Type: Human Prescription Drug
Drug Name:  Nplate
Dosage Form: Subcutaneous Injection, Powder, Lyophilized, for Solution
Application #: BLA125268
Rev. Date: 


NDC Package Codes:

  • 55513-221-01: 1 VIAL IN 1 CARTON (55513‑221‑01) > .5 ML IN 1 VIAL

Active Ingredients:

  • Romiplostim

Dosage Strength:

  • 250 ug/.5mL

Pharmaceutical Classes:

  • Increased Megakaryocyte Maturation [PE]
  • Increased Platelet Production [PE]
  • Thrombopoietin Receptor Agonist [EPC]
  • Thrombopoietin Receptor Agonists [MoA]

Related Products:

Based on records with the same trade name.
  • 55513-222 Nplate 500 ug/ml Subcutaneous Injection, Powder, Lyophilized, for Solution by Amgen Inc
  • 55513-223 Nplate 125 mg/.25ml Subcutaneous Injection, Powder, Lyophilized, for Solution by Amgen Inc

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Related Discussions:

Questions about the Side effect/reaction for long terms of Romiplostim use.
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.