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 3 of 4 · 80 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
YVTYVT MICRODERMABRASION FACIAL SCRUBYVTYVT MICRODERMABRASION FACIAL SCRUBBeijing JUNGE Technology Co., Ltd.2f30fc45-42e2-c766-e063-6394a90a8d682025-02-28WarningsExact identifier
unii: OP1R32D61U
SucralfateSUCRALFATECoupler LLC2d586736-73ae-9af0-e063-6294a90ad8752025-02-04Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATE ORALPrecision Dose, Inc.0dc592e9-541c-4fac-8ab5-829d43521c012025-01-28Warnings, Adverse reactionsExact identifier
unii: XX73205DH5
SucralfateSUCRALFATEDirect_Rxf5f0fecb-949c-3998-e053-2a95a90aac8c2025-01-22Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SUCRALFATESUCRALFATEDIRECT RXc50b5044-31ed-672a-e053-2995a90a49fc2025-01-20Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATENuCare Pharmaceuticals,Inc.0206d7fa-a1d5-35d9-e063-6294a90a5eb32025-01-03Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATEAdvanced Rx of Tennessee, LLCb39f22c8-f224-451a-e053-2995a90aaad72024-12-31Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATEAdvanced Rx Pharmacy of Tennessee, LLCd3c41720-7e1a-08c1-e053-2a95a90aba032024-12-31Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATEAdvanced Rx Pharmacy of Tennessee, LLCf15fbb45-4406-0d32-e053-2995a90a40c52024-12-31Adverse reactionsExact identifier
application number: NDA018333
ndc (package): 80425-0213-1
ndc (product): 80425-0213
rxcui: 314234
spl id: 2a9a6113-0a2f-6005-e063-6294a90abc5e
spl set id: f15fbb45-4406-0d32-e053-2995a90a40c5
unii: XX73205DH5
SucralfateSUCRALFATECosette Pharmaceuticals, Inc.3054ce94-78a2-4da4-8b14-95311b412ab22024-11-25Warnings, Adverse reactionsExact identifier
unii: XX73205DH5
SucralfateSUCRALFATE ORALAmneal Pharmaceuticals LLC4350b771-76a9-4e00-93f0-a18c71288f832024-10-30Warnings, Adverse reactionsExact identifier
unii: XX73205DH5
SucralfateSUCRALFATEBryant Ranch Prepacka068e818-8da3-4f0d-88e0-acc88e76f3aa2024-08-22Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
1e1a3bb2-889e-9b31-e063-6394a90a306c115e8d00-8a63-f159-e063-6394a90a9dcc2024-07-25Adverse reactionsExact identifier
spl id: 1e1a3bb2-889e-9b31-e063-6394a90a306c
spl set id: 115e8d00-8a63-f159-e063-6394a90a9dcc
SucralfateSUCRALFATENuCare Pharmaceuticals,Inc.a40e43d4-9240-34ad-e053-2995a90a98e12024-07-15Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
CarafateSUCRALFATEAllergan, Inc.c87c6b50-6977-4fa7-ae98-40c0753f7aee2024-05-21Adverse reactionsExact identifier
application number: NDA018333
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATEProficient Rx LP51459cdb-a04a-49c2-8ee4-8f234f5224762024-05-01Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
Pure Cornstarch BabyCORN STARCHWalgreen Companyd0e9bd13-b568-4f7e-b036-8d23e71ad8bf2024-03-25WarningsExact identifier
unii: O8232NY3SJ
SucralfateSUCRALFATEAdvanced Rx Pharmacy of Tennessee, LLC138f0929-caad-56c6-e063-6294a90a55ef2024-03-13Adverse reactionsExact identifier
application number: NDA018333
ndc (package): 80425-0377-1
ndc (product): 80425-0377
rxcui: 314234
spl id: 138efa30-381b-353e-e063-6394a90ad4da
spl set id: 138f0929-caad-56c6-e063-6294a90a55ef
unii: XX73205DH5
SucralfateSUCRALFATEAmneal Pharmaceuticals NY LLCb2e07ac7-4a8a-4b68-bb65-167d1aa868832024-03-01Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATEBryant Ranch Prepack28d7d257-8545-4b9f-8412-8ba1445024002024-02-23Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5

Reported adverse events (FAERS/openFDA)#

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