16110-080 : Xolegel 20 mg/g Topical Gel


NDC: 16110-080
Labeler: Aqua Pharmaceuticals, LLC.
Product Type: Human Prescription Drug
Drug Name:  Xolegel
Dosage Form: Topical Gel
Application #: NDA021946
Rev. Date: 


NDC Package Codes:

  • 16110-080-02: 2 G IN 1 TUBE (16110‑080‑02)
  • 16110-080-45: 1 TUBE IN 1 CARTON (16110‑080‑45) > 45 G IN 1 TUBE

Active Ingredients:

  • Ketoconazole

Dosage Strength:

  • 20 mg/g

Pharmaceutical Classes:

  • Azole Antifungal [EPC]
  • Azoles [Chemical/Ingredient]
  • Cytochrome P450 3A4 Inhibitors [MoA]
  • Cytochrome P450 3A5 Inhibitors [MoA]
  • P-Glycoprotein Inhibitors [MoA]

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.