68083-412 : Cangrelor 50 mg Intravenous Injection, Powder, Lyophilized, for Solution


NDC: 68083-412
Labeler: Gland Pharma Limited
Product Type: Human Prescription Drug
Drug Name:  Cangrelor
Dosage Form: Intravenous Injection, Powder, Lyophilized, for Solution
Application #: ANDA213551
Rev. Date: 


NDC Package Codes:

  • 68083-412-10: 10 VIAL, SINGLE‑DOSE IN 1 CARTON (68083‑412‑10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION IN 1 VIAL, SINGLE‑DOSE

Active Ingredients:

  • Cangrelor

Dosage Strength:

  • 50 mg

Pharmaceutical Classes:

  • Decreased Platelet Aggregation [PE]
  • P2Y12 Platelet Inhibitor [EPC]
  • P2Y12 Receptor Antagonists [MoA]

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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.