NDC 80425-0091-01 - 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: 80425-0091
Requested NDC: 80425-0091-01
Package NDCs from labels: 80425-0091-1, 80425-0091-01
Manufacturer: Advanced Rx of Tennessee, LLC
Effective date: 2024-12-31
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Sucralfate - Advanced Rx of Tennessee, LLC	Advanced Rx of Tennessee, LLC	2024-12-31	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
80425-0091-1	Sucralfate	30 in 1 BOTTLE	TABLET	30		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
80425-0091	SUCRALFATE TABLET [ADVANCED RX OF TENNESSEE, LLC]	5	Current NDC, Legacy NDC, 1 package rows	20250101_b39f22c8-f224-451a-e053-2995a90aaad7.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
80425-0091-1	EA - Each	80425-0091	187cb544-ae9f-4e7a-b21a-eb980ad159f4	1	2023-06-06

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 · 67 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sucralfate	SUCRALFATE	Bryant Ranch Prepack	2687d670-8af6-42a2-9081-fee112e80fc0	2023-05-24	Adverse reactions	Exact identifier application number: ANDA070848 rxcui: 314234 unii: XX73205DH5
Sucralfate	SUCRALFATE	Bryant Ranch Prepack	370f5ac6-2c64-42ef-ab5d-075a473012f1	2023-05-22	Adverse reactions	Exact identifier rxcui: 314234 unii: XX73205DH5
Sucralfate	SUCRALFATE	A-S Medication Solutions	03b66f88-d346-4260-867c-c942c4c68a79	2023-05-02	Adverse reactions	Exact identifier rxcui: 314234 unii: XX73205DH5
Sucralfate	SUCRALFATE	Aphena Pharma Solutions - Tennessee, LLC	b414dc07-681c-4fde-965f-09df64c015e7	2021-05-19	Adverse reactions	Exact identifier rxcui: 314234 unii: XX73205DH5
Sucralfate	SUCRALFATE	Mylan Pharmaceuticals, Inc.	ae58c382-c1cf-4ebf-9c97-bdff0682df8b	2020-06-12	Adverse reactions	Exact identifier rxcui: 314234 unii: XX73205DH5
Sucralfate	SUCRALFATE	Aphena Pharma Solutions - Tennessee, LLC	84447e21-e311-4e9f-9065-53956e90135c	2019-04-22	Adverse reactions	Exact identifier rxcui: 314234 unii: XX73205DH5
Sucralfate	SUCRALFATE	Teva Pharmaceuticals USA, Inc.	c7a43df7-eb37-4273-9250-87953b1fd270	2015-09-01	Adverse reactions	Exact identifier application number: ANDA070848 ndc (product): 0093-2210 rxcui: 314234 spl id: c363786b-0fde-45c0-9575-2a4ca71aa592 spl set id: c7a43df7-eb37-4273-9250-87953b1fd270 unii: XX73205DH5

Reported adverse events (FAERS/openFDA)#

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