NDC 25682-022 – Ultomiris

Ravulizumab 300 mg/30mL · Solution, Concentrate · Intravenous

Human Prescription Drug

Product NDC25682-022

Product details

Brand name
Ultomiris
Generic name
Ravulizumab
Labeler
Alexion Pharmaceuticals Inc.
Dosage form
Solution, Concentrate
Route
Intravenous
Marketing category
BLA · BLA761108
Marketed since
December 21, 2018
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
25682-022-011 VIAL, GLASS in 1 CARTON (25682-022-01) / 30 mL in 1 VIAL, GLASSDec 21, 2018

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