NDC 50242-922 – Hemlibra

Emicizumab 105 mg/.7mL · Injection, Solution · Subcutaneous

Human Prescription Drug

Product NDC50242-922

Product details

Brand name
Hemlibra
Generic name
Emicizumab
Labeler
Genentech, Inc.
Dosage form
Injection, Solution
Route
Subcutaneous
Marketing category
BLA · BLA761083
Marketed since
November 16, 2017
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Hemlibra →

Package NDC codes (1)

Package NDCDescriptionSince
50242-922-011 VIAL, SINGLE-USE in 1 CARTON (50242-922-01) / .7 mL in 1 VIAL, SINGLE-USENov 16, 2017

Other Hemlibra products