antihemophilic factor, human recombinant residues 743-1636 deleted 1 UNT Injection
- RxCUI
- 1718993
- RxNorm name
- antihemophilic factor, human recombinant residues 743-1636 deleted 1 UNT Injection
- Display name
- antihemophilic factor, human recombinant residues 743-1636 deleted 1 UNT Injection
- Full name
- antihemophilic factor, human recombinant residues 743-1636 deleted 1 UNT Injection
- Term type
- PSN
- Status
- DailyMed mapping
- Updated
- 2026-06-04 23:38:58
Purple Book Biologic Products#
| BLA | Proprietary name | Proper name | License type | Status | Latest source |
|---|---|---|---|---|---|
| 125264 | Xyntha, Xyntha Solofuse | Antihemophilic Factor (Recombinant), Plasma/Albumin Free | 351(a) | Rx | 2026-09-01 |
UNII Substances#
No records found.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed RxNorm Mappings#
| Set ID | RxNorm mappings | Terms | SPL version | Label | Effective |
|---|---|---|---|---|---|
| 52e97c7f-8240-4cd6-afd2-c452ab2f6e32 | antihemophilic factor, human recombinant residues 743-1636 deleted 1 UNT Injection [PSN] · antihemophilic factor, human recombinant residues 743-1636 deleted 1 UNT Injection [SCD] · factor VIII, human recombinant residues 743-1636 deleted 1 UNT Injection [SY] | 3 | 33 | These highlights do not include all the information needed to use XYNTHA safely and effectively. See full prescribing information for XYNTHA. XYNTHA ® (antihemophilic factor [recombinant]) lyophilized powder for solution, for intravenous injection Initial U.S. Approval: 2008 | 20250227 |