54436-325 : Nocdurna 27.7 ug/1 Sublingual Tablet


NDC: 54436-325
Labeler: Antares Pharma, Inc.
Product Type: Human Prescription Drug
Drug Name:  Nocdurna
Dosage Form: Sublingual Tablet
Application #: NDA022517
Rev. Date: 


NDC Package Codes:

  • 54436-325-30: 3 BLISTER PACK IN 1 CARTON (54436‑325‑30) > 10 TABLET IN 1 BLISTER PACK (54436‑325‑10)

Active Ingredients:

  • Desmopressin Acetate

Dosage Strength:

  • 27.7 ug/1

Pharmaceutical Classes:

  • Factor VIII Activator [EPC]
  • Increased Coagulation Factor VIII Activity [PE]
  • Increased Coagulation Factor VIII Concentration [PE]
  • Vasopressin Analog [EPC]
  • Vasopressins [CS]

Related Products:

Based on records with the same trade name.
  • 54436-350 Nocdurna 55.3 ug/1 Sublingual Tablet by Antares Pharma, Inc.
  • 55566-5050 Nocdurna 27.7 ug/1 Sublingual Tablet by Ferring Pharmaceuticals Inc.
  • 55566-5070 Nocdurna 55.3 ug/1 Sublingual Tablet by Ferring Pharmaceuticals Inc.

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.