SUCRALFATE - Food and Drug Administration
- Manufacturer
- Food and Drug Administration
- Effective date
- 2024-05-08
- Label type
- Indexing - Product Concept
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-05 00:23:59
Label at a glance#
ProductSUCRALFATE
Active ingredientSUCRALFATE
Products#
Every source-derived product name is available through these pages.
- SUCRALFATE
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SUCRALFATE | XX73205DH5 | ACTIB |
Source Document#
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 |
|---|---|---|---|---|---|---|
| Sucralfate | SUCRALFATE | Bryant Ranch Prepack | 2687d670-8af6-42a2-9081-fee112e80fc0 | 2023-05-24 | Adverse reactions | Sucralfate SUCRALFATE |
| Sucralfate | SUCRALFATE | Bryant Ranch Prepack | 370f5ac6-2c64-42ef-ab5d-075a473012f1 | 2023-05-22 | Adverse reactions | Sucralfate SUCRALFATE |
| Sucralfate | SUCRALFATE | A-S Medication Solutions | 03b66f88-d346-4260-867c-c942c4c68a79 | 2023-05-02 | Adverse reactions | Sucralfate SUCRALFATE |
| Sucralfate | SUCRALFATE | Aphena Pharma Solutions - Tennessee, LLC | b414dc07-681c-4fde-965f-09df64c015e7 | 2021-05-19 | Adverse reactions | Sucralfate SUCRALFATE |
| Sucralfate | SUCRALFATE | Mylan Pharmaceuticals, Inc. | ae58c382-c1cf-4ebf-9c97-bdff0682df8b | 2020-06-12 | Adverse reactions | Sucralfate SUCRALFATE |
| Sucralfate | SUCRALFATE | Aphena Pharma Solutions - Tennessee, LLC | 84447e21-e311-4e9f-9065-53956e90135c | 2019-04-22 | Adverse reactions | Sucralfate SUCRALFATE |
| Sucralfate | SUCRALFATE | Teva Pharmaceuticals USA, Inc. | c7a43df7-eb37-4273-9250-87953b1fd270 | 2015-09-01 | Adverse reactions | Sucralfate SUCRALFATE |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.