13533-613 : Plasmanate 2.5 g/50ml Intravenous Solution


NDC13533-613
Labeler: Grifols USA, LLC
Product Type: Plasma Derivative
Drug Name:  Plasmanate
Dosage Form: Intravenous Solution
Application #: BLA101140
Rev. Date: 


NDC Package Codes:

  • 13533-613-20: 1 VIAL IN 1 CARTON (13533‑613‑20) > 50 ML IN 1 VIAL (13533‑613‑21)
  • 13533-613-25: 1 VIAL IN 1 CARTON (13533‑613‑25) > 250 ML IN 1 VIAL (13533‑613‑26)
  • 13533-613-27: 1 VIAL IN 1 CARTON (13533‑613‑27) > 500 ML IN 1 VIAL (13533‑613‑28)

Active Ingredients:

  • Albumin Human

Dosage Strength:

  • 2.5 g/50mL

Pharmaceutical Classes:

  • Human Serum Albumin [EPC]
  • Increased Intravascular Volume [PE]
  • Increased Oncotic Pressure [PE]
  • Osmotic Activity [MoA]
  • Serum Albumin [Chemical/Ingredient]

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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.