70121-2701 : Oziltus 70 mg/ml Subcutaneous Injection, Solution


NDC: 70121-2701
Labeler: Amneal Pharmaceuticals LLC
Product Type: Human Prescription Drug
Drug Name:  Oziltus
Dosage Form: Subcutaneous Injection, Solution
Application #: BLA761457
Rev. Date: 


NDC Package Codes:

  • 70121-2701-1: 1 VIAL IN 1 CARTON (70121‑2701‑1) / 1.7 ML IN 1 VIAL

Active Ingredients:

  • Denosumab

Dosage Strength:

  • 70 mg/mL

Pharmaceutical Classes:

  • RANK Ligand Blocking Activity [MoA]
  • RANK Ligand Inhibitor [EPC]

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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.