epoetin alfa-epbx 20000 UNT/ML Injectable Solution [Retacrit]
- RxCUI
- 2463737
- RxNorm name
- epoetin alfa-epbx 20000 UNT/ML Injectable Solution [Retacrit]
- Display name
- epoetin alfa-epbx 20000 UNT/ML Injectable Solution [Retacrit]
- Full name
- epoetin alfa-epbx 20000 UNT/ML Injectable Solution [Retacrit]
- Term type
- SBD
- Status
- DailyMed mapping
- Updated
- 2026-06-04 23:38:54
Purple Book Biologic Products#
| BLA | Proprietary name | Proper name | License type | Status | Latest source |
|---|---|---|---|---|---|
| 125545 | Retacrit | epoetin alfa-epbx | 351(k) Biosimilar | Rx | 2026-07-01 |
UNII Substances#
No records found.
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| RETACRIT | EPOETIN ALFA-EPBX | Vifor (International) Inc. | e6e4dd0c-25ca-40b2-ba6b-6138a68621fe | 2025-06-22 | Boxed warning, Warnings, Adverse reactions | 2463737 |
| RETACRIT | EPOETIN ALFA-EPBX | Pfizer Laboratories Div Pfizer Inc | 3af26b0d-8ad0-44e1-a538-8bdb5ab39374 | 2025-06-22 | Boxed warning, Warnings, Adverse reactions | 2463737 |
DailyMed RxNorm Mappings#
| Set ID | RxNorm mappings | Terms | SPL version | Label | Effective |
|---|---|---|---|---|---|
| 3af26b0d-8ad0-44e1-a538-8bdb5ab39374 | Retacrit 20,000 UNT/ML Injectable Solution [PSN] · epoetin alfa-epbx 20000 UNT/ML Injectable Solution [Retacrit] [SBD] · EPO-epbx 20000 UNT/ML Injectable Solution [Retacrit] [SY] · ERYTHROPOIETIN-epbx 20000 UNT/ML Injectable Solution [Retacrit] [SY] · Retacrit 20000 UNT/ML Injectable Solution [SY] | 5 | 19 | These highlights do not include all the information needed to use RETACRIT safely and effectively. See full prescribing information for RETACRIT. RETACRIT ® (epoetin alfa-epbx) injection, for intravenous or subcutaneous use Initial U.S. Approval: 2018 RETACRIT (epoetin alfa-epbx) is biosimilar Biosimilar means that the biological product is approved based on data demonstrating that it is highly similar to an FDA-approved biological product, known as a reference product, and that there are no clinically mean | 20250622 |
| e6e4dd0c-25ca-40b2-ba6b-6138a68621fe | Retacrit 20,000 UNT/ML Injectable Solution [PSN] · epoetin alfa-epbx 20000 UNT/ML Injectable Solution [Retacrit] [SBD] · EPO-epbx 20000 UNT/ML Injectable Solution [Retacrit] [SY] · ERYTHROPOIETIN-epbx 20000 UNT/ML Injectable Solution [Retacrit] [SY] · Retacrit 20000 UNT/ML Injectable Solution [SY] | 5 | 14 | These highlights do not include all the information needed to use RETACRIT safely and effectively. See full prescribing information for RETACRIT. RETACRIT ® (epoetin alfa-epbx) injection, for intravenous or subcutaneous use Initial U.S. Approval: 2018 RETACRIT (epoetin alfa-epbx) is biosimilar Biosimilar means that the biological product is approved based on data demonstrating that it is highly similar to an FDA-approved biological product, known as a reference product, and that there are no clinically mean | 20250622 |