50242-921 : Hemlibra 150 mg/ml Subcutaneous Injection, Solution


NDC50242-921
Labeler: Genentech, Inc.
Product Type: Human Prescription Drug
Drug Name:  Hemlibra
Dosage Form: Subcutaneous Injection, Solution
Application #: BLA761083
Rev. Date: 


NDC Package Codes:

  • 50242-921-01: 1 VIAL, SINGLE‑USE IN 1 CARTON (50242‑921‑01) > .4 ML IN 1 VIAL, SINGLE‑USE

Active Ingredients:

  • Emicizumab

Dosage Strength:

  • 150 mg/mL

Related Products:

Based on records with the same trade name.
  • 50242-920 Hemlibra 30 mg/ml Subcutaneous Injection, Solution by Genentech, Inc.
  • 50242-922 Hemlibra 150 mg/ml Subcutaneous Injection, Solution by Genentech, Inc.
  • 50242-923 Hemlibra 150 mg/ml Subcutaneous Injection, Solution by Genentech, Inc.
  • 50242-927 Hemlibra 12 mg/.4ml Subcutaneous Injection, Solution by Genentech, Inc.
  • 50242-930 Hemlibra 300 mg/2ml Subcutaneous Injection, Solution by Genentech, Inc.

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