50242-137 : Actemra 20 mg/ml Intravenous Injection, Solution, Concentrate


NDC50242-137
Labeler: Genentech, Inc.
Product Type: Human Prescription Drug
Drug Name:  Actemra
Dosage Form: Intravenous Injection, Solution, Concentrate
Application #: BLA125276
Rev. Date: 


NDC Package Codes:

  • 50242-137-01: 1 VIAL, SINGLE‑USE IN 1 BOX (50242‑137‑01) > 20 ML IN 1 VIAL, SINGLE‑USE
  • 50242-137-04: 4 VIAL, SINGLE‑USE IN 1 BOX (50242‑137‑04) > 20 ML IN 1 VIAL, SINGLE‑USE

Active Ingredients:

  • Tocilizumab

Dosage Strength:

  • 20 mg/mL

Pharmaceutical Classes:

  • Interleukin 6 Receptor Antagonists [MoA]
  • Interleukin-6 Receptor Antagonist [EPC]

Related Products:

Based on records with the same trade name.
  • 50242-135 Actemra 20 mg/ml Intravenous Injection, Solution, Concentrate by Genentech, Inc.
  • 50242-136 Actemra 20 mg/ml Intravenous Injection, Solution, Concentrate by Genentech, Inc.
  • 50242-138 Actemra 180 mg/ml Subcutaneous Injection, Solution by Genentech, Inc.

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Related Discussions:

Swollen and tender legs from Actemra?
My wife has been on Actemra for about 6-7months now and her doctor says it's working, my wife disagrees. Due to her ... 5 replies




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