Stimufend Purple Book BLA 761173
- BLA number
- 761173
- Proprietary names
- Stimufend
- Proper names
- pegfilgrastim-fpgk
- Applicant
- Fresenius Kabi USA, LLC
- Center
- CDER
- First observed release
- 2022-09-01
- 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 | Stimufend | pegfilgrastim-fpgk | 351(k) Biosimilar | 6MG/0.6ML | Injection | Subcutaneous | Pre-Filled Syringe | Rx | Licensed | 2022-09-01 | |
Reference Biological Product#
BLA, Proprietary name, Proper name table| BLA | Proprietary name | Proper name | License type | Status | Latest source |
|---|
| 125031 | Neulasta | pegfilgrastim | 351(a) | Rx | 2026-06-01 |
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 |
|---|
| 2022-09-01 | N | 001 | Stimufend | 351(k) Biosimilar | Rx | Fresenius Kabi USA, LLC |
Observed Product State History#
Release, Product, Name table| Release | Product | Name | License type | Marketing | Licensure | Approval |
|---|
| 2022-09-01 | 001 | Stimufend | 351(k) Biosimilar | Rx | Licensed | 2022-09-01 |