NDC 00591-0780 - Sucralfate
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 00591-0780
- Manufacturer
- State of Florida DOH Central Pharmacy
- Effective date
- 2010-06-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Sucralfate - State of Florida DOH Central Pharmacy | State of Florida DOH Central Pharmacy | 2010-06-08 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| SUCRALFATE | ACTIVE INGREDIENT | XX73205DH5 | SUCRALFATE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 1 | |
| SUCRALFATE | ACTIVE MOIETY | XX73205DH5 | SUCRALFATE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | SUCRALFATE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | SUCRALFATE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | SUCRALFATE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 1 |
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 | 25ae2ebc-a7e0-4fc9-a8d1-07f7dd7138e5 | 2024-01-11 | Adverse reactions | 314234 XX73205DH5 |
| Sucralfate | SUCRALFATE | Proficient Rx LP | a42c5f3d-85f1-485b-91e6-58c25b3ddc71 | 2024-01-01 | Adverse reactions | 314234 XX73205DH5 |
| Sucralfate | SUCRALFATE | Amneal Pharmaceuticals NY LLC | a4f722e7-2885-4f27-8358-9c662439600a | 2023-12-30 | Adverse reactions | 314234 XX73205DH5 |
| Sucralfate | SUCRALFATE | American Health Packaging | e4761fb2-6a1a-44de-9d27-f6addabc24c8 | 2023-08-10 | Warnings, Adverse reactions | XX73205DH5 |
| Sucralfate | SUCRALFATE | A-S Medication Solutions | 793d033d-d341-4910-8dda-d43d8fd03a4d | 2023-06-29 | Adverse reactions | NDA018333 314234 XX73205DH5 |
| Carafate | SUCRALFATE | Allergan, Inc. | 0fb67b1c-b4c0-46f2-8a81-df1510e006aa | 2023-06-08 | Warnings, Adverse reactions | XX73205DH5 |
| Sucralfate | SUCRALFATE | Bryant Ranch Prepack | 2687d670-8af6-42a2-9081-fee112e80fc0 | 2023-05-24 | Adverse reactions | 314234 XX73205DH5 |
| Sucralfate | SUCRALFATE | Bryant Ranch Prepack | 370f5ac6-2c64-42ef-ab5d-075a473012f1 | 2023-05-22 | Adverse reactions | 314234 XX73205DH5 |
| Sucralfate | SUCRALFATE | A-S Medication Solutions | 03b66f88-d346-4260-867c-c942c4c68a79 | 2023-05-02 | Adverse reactions | 314234 XX73205DH5 |
| Sucralfate | SUCRALFATE | Aphena Pharma Solutions - Tennessee, LLC | b414dc07-681c-4fde-965f-09df64c015e7 | 2021-05-19 | Adverse reactions | 314234 XX73205DH5 |
| Sucralfate | SUCRALFATE | Mylan Pharmaceuticals, Inc. | ae58c382-c1cf-4ebf-9c97-bdff0682df8b | 2020-06-12 | Adverse reactions | NDA018333 314234 XX73205DH5 |
| Sucralfate | SUCRALFATE | Aphena Pharma Solutions - Tennessee, LLC | 84447e21-e311-4e9f-9065-53956e90135c | 2019-04-22 | Adverse reactions | NDA018333 314234 XX73205DH5 |
| Sucralfate | SUCRALFATE | Teva Pharmaceuticals USA, Inc. | c7a43df7-eb37-4273-9250-87953b1fd270 | 2015-09-01 | Adverse reactions | 314234 XX73205DH5 |
| ecd35838-b551-4cc1-8cb2-2dc3335c61d4 | c48dda77-c4a6-4241-91dd-2cef599b0833 | 2010-06-08 | Adverse reactions | ecd35838-b551-4cc1-8cb2-2dc3335c61d4 c48dda77-c4a6-4241-91dd-2cef599b0833 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.