Tyenne Purple Book BLA 761275
- BLA number
- 761275
- Proprietary names
- Tyenne
- Proper names
- tocilizumab-aazg
- Applicant
- Fresenius Kabi USA, LLC
- Center
- CDER
- First observed release
- 2024-03-01
- Latest observed release
- 2026-06-01
- Newest archive release
- 2026-06-01
- FDA patent list
- No patents listed in the captured FDA patent list; source updated 2025-06-11
- Coverage
- Present in newest release
Latest Known Product Presentations#
Product, Proprietary name, Proper name table| Product | Proprietary name | Proper name | License type | Strength | Dosage form | Route | Presentation | Marketing | Licensure | Approval | Patent list provided |
|---|
| 001 | Tyenne | tocilizumab-aazg | 351(k) Biosimilar | 80MG/4ML (20MG/ML) | Injection | Intravenous | Single-Dose Vial | Rx | Licensed | 2024-03-05 | |
| 002 | Tyenne | tocilizumab-aazg | 351(k) Biosimilar | 200MG/10ML (20MG/ML) | Injection | Intravenous | Single-Dose Vial | Rx | Licensed | 2024-03-05 | |
| 003 | Tyenne | tocilizumab-aazg | 351(k) Biosimilar | 400MG/20ML (20MG/ML) | Injection | Intravenous | Single-Dose Vial | Rx | Licensed | 2024-03-05 | |
| 004 | Tyenne | tocilizumab-aazg | 351(k) Biosimilar | 162MG/0.9ML | Injection | Subcutaneous | Pre-Filled Syringe | Rx | Licensed | 2024-03-05 | |
| 005 | Tyenne | tocilizumab-aazg | 351(k) Biosimilar | 162MG/0.9ML | Injection | Subcutaneous | Autoinjector | Rx | Licensed | 2024-03-05 | |
Published Patent List#
No patents for this BLA were listed in the FDA Purple Book patent list captured from the source updated 2025-06-11.
Official Monthly Change Events#
Release, Event, Product table| Release | Event | Product | Name | License type | Status | Applicant |
|---|
| 2024-03-01 | N | 001 | Tyenne | 351(k) Biosimilar | Rx | Fresenius Kabi USA, LLC |
| 2024-03-01 | N | 002 | Tyenne | 351(k) Biosimilar | Rx | Fresenius Kabi USA, LLC |
| 2024-03-01 | N | 003 | Tyenne | 351(k) Biosimilar | Rx | Fresenius Kabi USA, LLC |
| 2024-03-01 | N | 004 | Tyenne | 351(k) Biosimilar | Rx | Fresenius Kabi USA, LLC |
| 2024-03-01 | N | 005 | Tyenne | 351(k) Biosimilar | Rx | Fresenius Kabi USA, LLC |
Observed Product State History#
Release, Product, Name table| Release | Product | Name | License type | Marketing | Licensure | Approval |
|---|
| 2024-03-01 | 001 | Tyenne | 351(k) Biosimilar | Rx | Licensed | 2024-03-05 |
| 2024-03-01 | 002 | Tyenne | 351(k) Biosimilar | Rx | Licensed | 2024-03-05 |
| 2024-03-01 | 003 | Tyenne | 351(k) Biosimilar | Rx | Licensed | 2024-03-05 |
| 2024-03-01 | 004 | Tyenne | 351(k) Biosimilar | Rx | Licensed | 2024-03-05 |
| 2024-03-01 | 005 | Tyenne | 351(k) Biosimilar | Rx | Licensed | 2024-03-05 |