NDC product
EMRELIS
NDC 0074-1044 · AbbVie Inc.
Key facts
| Product NDC | 0074-1044 |
|---|---|
| Proprietary name | EMRELIS |
| Nonproprietary name | Telisotuzumab Vedotin |
| Substances | TELISOTUZUMAB VEDOTIN |
| Dosage form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route | INTRAVENOUS |
| Labeler | AbbVie Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | BLA |
| Application number | BLA761384 |
| Marketing start | May 14, 2025 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: