Hemlibra
- Product NDC
- 50242-930
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- emicizumab
- Dosage form
- INJECTION, SOLUTION
- Route
- SUBCUTANEOUS
- Labeler
- Genentech, Inc.
- Application
- BLA761083
- Marketing category
- BLA
- Substance
- EMICIZUMAB
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50242-930-01 | 1 VIAL, SINGLE-USE in 1 CARTON (50242-930-01) / 2 mL in 1 VIAL, SINGLE-USE | 2023-03-16 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Hemlibra | Genentech, Inc. | F. Hoffmann-La Roche Ltd. | Roche Diagnostics | F. Hoffmann-La Roche AG | 2025-07-11 | HUMAN PRESCRIPTION DRUG LABEL | 17 |