NDC 25682-025 – Ultomiris

Ravulizumab 300 mg/3mL · Solution, Concentrate · Intravenous

Human Prescription Drug

Product NDC25682-025

Product details

Brand name
Ultomiris
Generic name
Ravulizumab
Labeler
Alexion Pharmaceuticals Inc.
Dosage form
Solution, Concentrate
Route
Intravenous
Marketing category
BLA · BLA761108
Marketed since
October 9, 2020
Listing expires
December 31, 2026
Pharmacologic class
Complement Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Ultomiris →

Package NDC codes (1)

Package NDCDescriptionSince
25682-025-011 VIAL, GLASS in 1 CARTON (25682-025-01) / 3 mL in 1 VIAL, GLASSOct 9, 2020

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