FDA.reportPublic FDA data

NDC 80425-0377-01 - 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
80425-0377
Requested NDC
80425-0377-01
Package NDCs from labels
80425-0377-1, 80425-0377-01
Manufacturer
Advanced Rx Pharmacy of Tennessee, LLC
Effective date
2024-03-13
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Sucralfate - Advanced Rx Pharmacy of Tennessee, LLCAdvanced Rx Pharmacy of Tennessee, LLC2024-03-13HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80425-0377-1Sucralfate30 in 1 BOTTLETABLET301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80425-0377SUCRALFATE TABLET [ADVANCED RX PHARMACY OF TENNESSEE, LLC]1Current NDC, 1 package rows20240315_138f0929-caad-56c6-e063-6294a90a55ef.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
80425-0377-1EA - Each80425-03777fb3f385-2b93-49dd-92a7-f896815397ef12024-04-05

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 · 76 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
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
rxcui: 314234
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
rxcui: 314234
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
YVTYVT MICRODERMABRASION FACIAL SCRUBYVTYVT MICRODERMABRASION FACIAL SCRUBBeijing JUNGE Technology Co., Ltd.2f30fc45-42e2-c766-e063-6394a90a8d682025-02-28WarningsExact identifier
unii: OP1R32D61U

Reported adverse events (FAERS/openFDA)#

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