23731-6051 : Anticoagulant Citrate Dextrose a Extracorporeal Solution


NDC: 23731-6051
Labeler: Citra Labs
Product Type: Human Prescription Drug
Drug Name: Anticoagulant Citrate Dextrose a
Dosage Form: Extracorporeal Solution
Application #: BN020037
Rev. Date: 


NDC Package Codes:

  • 23731-6051-1: 10 VIAL, SINGLE‑USE IN 1 CASE (23731‑6051‑1) > 30 ML IN 1 VIAL, SINGLE‑USE (23731‑6051‑3)
  • 23731-6051-2: 25 VIAL, SINGLE‑USE IN 1 CASE (23731‑6051‑2) > 30 ML IN 1 VIAL, SINGLE‑USE (23731‑6051‑3)
  • 23731-6051-3: 30 ML IN 1 VIAL, SINGLE‑USE (23731‑6051‑3)
  • 23731-6051-5: 12 BOTTLE, GLASS IN 1 BOX (23731‑6051‑5) > 50 ML IN 1 BOTTLE, GLASS

Active Ingredients:

  • Dextrose Monohydrate
  • Anhydrous Citric Acid
  • Trisodium Citrate Dihydrate

Dosage Strength:

  • .245 g/10mL
  • .073 g/10mL
  • .22 g/10mL

Pharmaceutical Classes:

  • Acidifying Activity [MoA]
  • Acidifying Activity [MoA]
  • Anti-coagulant [EPC]
  • Calcium Chelating Activity [MoA]
  • Calculi Dissolution Agent [EPC]
  • Decreased Coagulation Factor Activity [PE]

NDC QR Code

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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.