51862-376 : Sorilux 50 ug/g Topical Aerosol, Foam


NDC: 51862-376
Labeler: Mayne Pharma LLC
Product Type: Human Prescription Drug
Drug Name:  Sorilux
Dosage Form: Topical Aerosol, Foam
Application #: NDA022563
Rev. Date: 


NDC Package Codes:

  • 51862-376-12: 1 CAN IN 1 CARTON (51862‑376‑12) > 120 G IN 1 CAN
  • 51862-376-60: 1 CAN IN 1 CARTON (51862‑376‑60) > 60 G IN 1 CAN

Active Ingredients:

  • Calcipotriene

Dosage Strength:

  • 50 ug/g

Pharmaceutical Classes:

  • Vitamin D [Chemical/Ingredient]
  • Vitamin D Analog [EPC]

Related Products:

Based on records with the same trade name.
  • 0145-2130 Sorilux 50 ug/g Topical Aerosol, Foam by Stiefel Laboratories Inc

NDC QR Code

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NDC 51862-376 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.