FDA.reportPublic FDA data

NDC 69238-1656-01 - 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
69238-1656
Requested NDC
69238-1656-01
Package NDCs from labels
69238-1656-1, 69238-1656-5, 69238-1656-01
Manufacturer
AvKARE
Effective date
2026-01-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Sucralfate - AvKAREAvKARE2026-01-19HUMAN PRESCRIPTION DRUG LABEL
Sucralfate Tablets, USPAmneal Pharmaceuticals NY LLC | Amneal Pharmaceuticals of New York, LLC2023-12-30HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69238-1656-1Sucralfate100 in 1 BOTTLETABLET1006
69238-1656-5Sucralfate500 in 1 BOTTLETABLET5006

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69238-1656SUCRALFATE TABLET [AMNEAL PHARMACEUTICALS NY LLC]6Current NDC, Legacy NDC, 2 package rows20231231_a4f722e7-2885-4f27-8358-9c662439600a.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69238-1656-1EA - Each69238-1656247e0143-e808-4a3c-8fa8-02bb11c5d6cb12022-07-06

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 · 73 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SucralfateSUCRALFATEAvKARE0909acc5-c746-17fb-e063-6394a90a677f2026-01-19Adverse reactionsExact identifier
application number: ANDA215576
ndc (package): 42291-936-90
ndc (product): 42291-936
rxcui: 314234
spl id: 48c0e47e-08b1-0c73-e063-6394a90a90b7
spl set id: 0909acc5-c746-17fb-e063-6394a90a677f
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
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
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.