0023-5858 : Liletta 52 mg Intrauterine Intrauterine Device


NDC: 0023-5858
Labeler: Allergan, Inc.
Product Type: Human Prescription Drug
Drug Name:  Liletta
Dosage Form: Intrauterine Intrauterine Device
Application #: NDA206229
Rev. Date: 


NDC Package Codes:

  • 0023-5858-01: 1 TRAY IN 1 CARTON (0023‑5858‑01) > 1 INTRAUTERINE DEVICE IN 1 TRAY

Active Ingredients:

  • Levonorgestrel

Dosage Strength:

  • 52 mg

Pharmaceutical Classes:

  • Inhibit Ovum Fertilization [PE]
  • Progesterone Congeners [CS]
  • Progestin [EPC]
  • Progestin-containing Intrauterine Device [EPC]

Related Products:

Based on records with the same trade name.
  • 52544-035 Liletta 52 mg Intrauterine Intrauterine Device by Actavis Pharma, Inc.

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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.