82292-040 : Lumisight 10 mg/ml Intravenous Injection, Powder, Lyophilized, for Solution


NDC: 82292-040
Labeler: Lumicell, Inc.
Product Type: Human Prescription Drug
Drug Name:  Lumisight
Dosage Form: Intravenous Injection, Powder, Lyophilized, for Solution
Application #: NDA214511
Rev. Date: 


NDC Package Codes:

  • 82292-040-10: 10 VIAL IN 1 CARTON (82292‑040‑10) / 3.9 ML IN 1 VIAL (82292‑040‑01)

Active Ingredients:

  • Pegulicianine

Dosage Strength:

  • 10 mg/mL

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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.