FDA.reportPublic FDA data

NDC 59762-0401-01 - 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
59762-0401
Requested NDC
59762-0401-01
Package NDCs from labels
59762-0401-1, 59762-0401-5, 59762-0401-01
Manufacturer
Preferred Pharmaceuticals Inc.
Effective date
2026-09-02
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Sucralfate TabletsPreferred Pharmaceuticals Inc.2026-09-02HUMAN PRESCRIPTION DRUG LABEL
Sucralfate TabletsREMEDYREPACK INC.2026-06-11HUMAN PRESCRIPTION DRUG LABEL
Sucralfate - Northwind Health Company, LLCNorthwind Health Company, LLC2026-01-01HUMAN PRESCRIPTION DRUG LABEL
Sucralfate - Bryant Ranch PrepackBryant Ranch Prepack2025-06-02HUMAN PRESCRIPTION DRUG LABEL
Sucralfate - Advanced Rx Pharmacy of Tennessee, LLCAdvanced Rx Pharmacy of Tennessee, LLC2024-12-31HUMAN PRESCRIPTION DRUG LABEL
Sucralfate - Redpharm drugRedpharm drug2024-07-25HUMAN PRESCRIPTION DRUG LABEL
Sucralfate - Advanced Rx Pharmacy of Tennessee, LLCAdvanced Rx Pharmacy of Tennessee, LLC2024-03-13HUMAN PRESCRIPTION DRUG LABEL
Sucralfate - A-S Medication SolutionsA-S Medication Solutions2023-06-29HUMAN PRESCRIPTION DRUG LABEL
Sucralfate - Denton Pharma, Inc. DBA Northwind PharmaceuticalsDenton Pharma, Inc. DBA Northwind Pharmaceuticals2023-01-01HUMAN PRESCRIPTION DRUG LABEL
Sucralfate TabletsMylan Pharmaceuticals, Inc.2020-06-12HUMAN PRESCRIPTION DRUG LABEL
Sucralfate - Denton Pharma, Inc. DBA Northwind PharmaceuticalsDenton Pharma, Inc. DBA Northwind Pharmaceuticals2020-06-08HUMAN PRESCRIPTION DRUG LABEL
Sucralfate - Aphena Pharma Solutions - Tennessee, LLCAphena Pharma Solutions - Tennessee, LLC2019-04-22HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59762-0401-1Sucralfate100 in 1 BOTTLETABLET1008
59762-0401-5Sucralfate500 in 1 BOTTLETABLET5008

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59762-0401SUCRALFATE TABLET [GREENSTONE LLC]7Current NDC, Legacy NDC, 2 package rows20241109_ae58c382-c1cf-4ebf-9c97-bdff0682df8b.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59762-0401-1EA - Each59762-04013ddd04f4-562e-4166-9142-62d72866d96612017-11-06
59762-0401-5EA - Each59762-04013a24233e-7ccb-4d0b-bef5-dc157a1d750812017-11-06

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.

Matched openFDA labels page 2 of 4 · 80 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SucralfateSUCRALFATEPreferred Pharmaceuticals Inca434bf8f-cc60-4d84-a9a4-61c3ff6b700e2026-01-21Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATEAvKARE0909acc5-c746-17fb-e063-6394a90a677f2026-01-19Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
Lotrimin Daily Sweat and Odor ControlTOPICAL STARCHBayer HealthCare LLC.9ec5c80d-b550-496f-e053-2a95a90a54892026-01-16WarningsExact identifier
unii: O8232NY3SJ
Sucralfate oral suspensionSUCRALFATEGlenmark Pharmaceuticals Inc., USA1e595c2a-edd0-43f7-a2db-69553b9557d92026-01-06Warnings, Adverse reactionsExact identifier
unii: XX73205DH5
SucralfateSUCRALFATENorthwind Health Company, LLCf3095db3-fd02-873c-e053-2a95a90a5b1f2026-01-01Adverse reactionsExact identifier
application number: NDA018333
ndc (package): 51655-475-52
ndc (product): 51655-475
rxcui: 314234
spl id: 490f38ea-fc45-7aa2-e063-6294a90a9f1c
spl set id: f3095db3-fd02-873c-e053-2a95a90a5b1f
unii: XX73205DH5
SucralfateSUCRALFATE ORALTruPharma, LLC7d441128-45d2-4bf2-817b-665784992e902025-12-29Warnings, Adverse reactionsExact identifier
unii: XX73205DH5
Medicated Cornstarch Baby PowderACTIVE CORN STARCHDavion, Inc.e39032d1-c8cd-4a41-af10-126970b8ad382025-12-29WarningsExact identifier
unii: O8232NY3SJ
SucralfateSUCRALFATENorthwind Health Company, LLC464bf611-4dbb-4707-b9dd-39ca178ed4bf2025-12-26Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATERedpharm Drug3251e156-4c52-63b3-e063-6294a90a9a952025-12-18Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATE ORALAvKAREc019bf24-8273-8d2f-e053-2a95a90aec982025-12-03Warnings, Adverse reactionsExact identifier
unii: XX73205DH5
SucralfateSUCRALFATE ORALAvPAKe78ef7d4-faa7-aebf-e053-2995a90a6f842025-12-03Warnings, Adverse reactionsExact identifier
unii: XX73205DH5
SucralfateSUCRALFATETorrent Pharmaceuticals Limiteddc361b46-fda4-4b0b-9950-e8885ba5b0842025-08-21Warnings, Adverse reactionsExact identifier
unii: XX73205DH5
SucralfateSUCRALFATEMylan Institutional Inc.989ca8a8-3ad6-4ee4-aa9c-eed7318287532025-07-22Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATEKesin Pharma Corporation36d940f2-207b-68c5-e063-6294a90a6b4a2025-07-01Warnings, Adverse reactionsExact identifier
unii: XX73205DH5
SucralfateSUCRALFATENCS HealthCare of KY, LLC dba Vangard Labsd67dcaad-56c1-4e77-a0c8-6559708084142025-06-13Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATEBryant Ranch Prepacka73010fb-960c-4567-8ab1-6d902fee2c142025-06-02Adverse reactionsExact identifier
application number: NDA018333
ndc (package): 71335-2637-6
ndc (package): 71335-2637-7
ndc (package): 71335-2637-2
ndc (package): 71335-2637-9
ndc (package): 71335-2637-1
ndc (package): 71335-2637-8
ndc (package): 71335-2637-3
ndc (package): 71335-2637-4
ndc (package): 71335-2637-0
ndc (product): 71335-2637
rxcui: 314234
spl id: dc7f253b-f40a-4774-8456-1d383fb35b0c
spl set id: a73010fb-960c-4567-8ab1-6d902fee2c14
unii: XX73205DH5
SucralfateSUCRALFATEATLANTIC BIOLOGICALS CORP.e5073597-ac51-4e7c-a9dc-7695773a01f12025-05-27Warnings, Adverse reactionsExact identifier
unii: XX73205DH5
SucralfateSUCRALFATERichmond Pharmaceuticals, Inc.7ac10c3f-9d50-4702-900c-41075ac6f8962025-05-23Warnings, Adverse reactionsExact identifier
unii: XX73205DH5
sucralfateSUCRALFATEBryant Ranch Prepackabc44549-ac41-4aef-9b15-2ba536e1555f2025-05-09Warnings, Adverse reactionsExact identifier
unii: XX73205DH5
SucralfateSUCRALFATENuCare Pharmaceuticals, Inc.31a7dcd0-e677-249a-e063-6294a90a75f62025-03-19Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.