NDC 0074-1044 – Emrelis

Telisotuzumab Vedotin 20 mg/mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug

Product NDC0074-1044

Product details

Brand name
Emrelis
Generic name
Telisotuzumab Vedotin
Labeler
AbbVie Inc.
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
BLA · BLA761384
Marketed since
May 14, 2025
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Emrelis →

Package NDC codes (1)

Package NDCDescriptionSince
0074-1044-011 VIAL, SINGLE-DOSE in 1 CARTON (0074-1044-01) / 1 mL in 1 VIAL, SINGLE-DOSEMay 14, 2025

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