Reopro Purple Book BLA 103575
- BLA number
- 103575
- Proprietary names
- Reopro
- Proper names
- abciximab
- Applicant
- Janssen Biotech, Inc.
- Center
- CDER
- First observed release
- 2020-05-01
- 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 | Reopro | abciximab | 351(a) | 2MG/ML | Injection | Intravenous | Single-Dose Vial | Disc | Voluntarily Revoked | 1994-12-22 | |
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 |
|---|
| 2020-05-01 | R | 001 | Reopro | 351(a) | Disc | Janssen Biotech, Inc. |
Observed Product State History#
Release, Product, Name table| Release | Product | Name | License type | Marketing | Licensure | Approval |
|---|
| 2020-10-01 | 001 | Reopro | 351(a) | Disc | Voluntarily Revoked | 1994-12-22 |
| 2020-09-01 | 001 | Dysport | 351(a) | Rx | Licensed | 2009-04-29 |
| 2020-05-01 | 001 | Reopro | 351(a) | Disc | Voluntarily Revoked | 1994-12-22 |