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 4 of 4 · 73 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SucralfateSUCRALFATEBryant Ranch Prepack25ae2ebc-a7e0-4fc9-a8d1-07f7dd7138e52024-01-11Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATEProficient Rx LPa42c5f3d-85f1-485b-91e6-58c25b3ddc712024-01-01Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATEAmneal Pharmaceuticals NY LLCa4f722e7-2885-4f27-8358-9c662439600a2023-12-30Adverse reactionsExact identifier
application number: ANDA215576
ndc (package): 69238-1656-5
ndc (package): 69238-1656-1
ndc (product): 69238-1656
ndc11 (package): 69238165601
rxcui: 314234
spl id: 507ba68d-7593-4545-bbe1-dc9463c1a893
spl set id: a4f722e7-2885-4f27-8358-9c662439600a
unii: XX73205DH5
SucralfateSUCRALFATEAmerican Health Packaginge4761fb2-6a1a-44de-9d27-f6addabc24c82023-08-10Warnings, Adverse reactionsExact identifier
unii: XX73205DH5
SucralfateSUCRALFATEA-S Medication Solutions793d033d-d341-4910-8dda-d43d8fd03a4d2023-06-29Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
CarafateSUCRALFATEAllergan, Inc.0fb67b1c-b4c0-46f2-8a81-df1510e006aa2023-06-08Warnings, Adverse reactionsExact identifier
unii: XX73205DH5
SucralfateSUCRALFATEBryant Ranch Prepack2687d670-8af6-42a2-9081-fee112e80fc02023-05-24Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATEBryant Ranch Prepack370f5ac6-2c64-42ef-ab5d-075a473012f12023-05-22Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATEA-S Medication Solutions03b66f88-d346-4260-867c-c942c4c68a792023-05-02Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATEAphena Pharma Solutions - Tennessee, LLCb414dc07-681c-4fde-965f-09df64c015e72021-05-19Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATEMylan Pharmaceuticals, Inc.ae58c382-c1cf-4ebf-9c97-bdff0682df8b2020-06-12Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATEAphena Pharma Solutions - Tennessee, LLC84447e21-e311-4e9f-9065-53956e90135c2019-04-22Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5
SucralfateSUCRALFATETeva Pharmaceuticals USA, Inc.c7a43df7-eb37-4273-9250-87953b1fd2702015-09-01Adverse reactionsExact identifier
rxcui: 314234
unii: XX73205DH5

Reported adverse events (FAERS/openFDA)#

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