50222-499 : Taclonex Topical Suspension

Labeler: Leo Pharma Inc.
Product Type: Human Prescription Drug
Drug Name:  Taclonex
Dosage Form: Topical Suspension
Application #: NDA022185
Rev. Date: 

NDC Package Codes:

  • 50222-499-60: 1 APPLICATOR IN 1 CARTON (50222‑499‑60) > 60 G IN 1 APPLICATOR

Active Ingredients:

  • Calcipotriene Hydrate
  • Betamethasone Dipropionate

Dosage Strength:

  • 50 ug/g
  • .5 mg/g

Pharmaceutical Classes:

  • Vitamin D [Chemical/Ingredient]
  • Vitamin D Analog [EPC]
  • Corticosteroid [EPC]
  • Corticosteroid Hormone Receptor Agonists [MoA]

Related Products:

Based on records with the same trade name.
  • 50222-227 Taclonex Topical Ointment by Leo Pharma Inc.
  • 50222-501 Taclonex Topical Suspension by Leo Pharma Inc.
  • 0430-3230 Taclonex Topical Ointment by Warner Chilcott (Us), LLC
  • 54868-5680 Taclonex Topical Ointment by Physicians Total Care, Inc.


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Note: The MedsChat® 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.