NDC 57926-464-31 - Salix

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: 57926-464
Requested NDC: 57926-464-31
Package NDCs from labels: 57926-464-31
Manufacturer: Merck Sharp & Dohme Corp.
Effective date: 2025-10-30
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Salix ® (furosemide tablets)	Merck Sharp & Dohme Corp.	2025-10-30	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
57926-464-31	Salix	500 in 1 BOTTLE	TABLET	500		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
57926-464	SALIX (FUROSEMIDE) TABLET [MERCK SHARP & DOHME CORP.]	6	1 package rows	20250503_9ad8eb8a-7c65-4746-9c03-1d6136b5892c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Furosemide	ACTIVE INGREDIENT	7LXU5N7ZO5	SALIX (FUROSEMIDE) TABLET [SCHERING CORPORATION]	1
Furosemide	ACTIVE MOIETY	7LXU5N7ZO5	SALIX (FUROSEMIDE) TABLET [SCHERING CORPORATION]	1
Cellulose, Microcrystalline	INACTIVE INGREDIENT	OP1R32D61U	SALIX (FUROSEMIDE) TABLET [SCHERING CORPORATION]	1
FD&C Yellow No. 5	INACTIVE INGREDIENT	I753WB2F1M	SALIX (FUROSEMIDE) TABLET [SCHERING CORPORATION]	1
Lactose Monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	SALIX (FUROSEMIDE) TABLET [SCHERING CORPORATION]	1
Magnesium Stearate	INACTIVE INGREDIENT	70097M6I30	SALIX (FUROSEMIDE) TABLET [SCHERING CORPORATION]	1
Starch, Corn	INACTIVE INGREDIENT	O8232NY3SJ	SALIX (FUROSEMIDE) TABLET [SCHERING CORPORATION]	1

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 1 of 8 · 159 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Furosemide	FUROSEMIDE	REMEDYREPACK INC.	dba00759-87b4-4ecf-998e-ba03ed3d2f1a	2026-08-17	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	Redpharm Drug	58d2a38d-75f8-dcb9-e063-6294a90a10d7	2026-08-12	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	Medical Purchasing Solutions, LLC	58cc1e38-6000-1489-e063-6394a90a5978	2026-08-11	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
FUROSCIX	FUROSEMIDE INJECTION 80 MG/ 10 ML	scPharmaceuticals Inc., a wholly owned subsidiary of MannKind Corporation	eac958dd-8d43-e44e-e053-2995a90a4d5e	2026-07-31	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	REMEDYREPACK INC.	7cdcd001-ab4b-4210-a455-2e17a7bc4972	2026-07-24	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	REMEDYREPACK INC.	3d312ab0-589c-427b-84da-18887244bfc9	2026-07-15	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	St. Mary's Medical Park Pharmacy	febeaf8c-0f4b-cc40-e053-6394a90a873e	2026-06-30	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	REMEDYREPACK INC.	916de29e-228c-4dfc-bcee-ad9a641316bd	2026-06-24	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	REMEDYREPACK INC.	e8c27f1c-dc81-44b1-8663-a7d663bad89f	2026-06-23	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	Atlantic Biologicals Corp.	54ed0dd9-2fa8-269a-e063-6294a90a607c	2026-06-23	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
FUROSEMIDE	FUROSEMIDE	HF Acquisition Co LLC, DBA HealthFirst	75d5611a-f9e0-1841-e053-2991aa0af415	2026-06-23	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	Unit Dose Solutions, Inc.	54dd664a-c7ec-27f3-e063-6294a90aff9f	2026-06-22	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	Cardinal Health 107, LLC	2a5bcf50-6d63-463a-915e-a72ea2e5f131	2026-06-18	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	Granulation Technology, Inc.	462e8917-cbe0-f4f9-e063-6394a90ab4ff	2026-06-17	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	Atlantic Biologicals Corps	9c342198-7162-4cc5-bda1-bc4054a4292b	2026-06-16	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	Coupler LLC	53e58232-f7f9-c09b-e063-6394a90a5bc4	2026-06-10	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	Cardinal Health 107, LLC	42478c55-9056-487a-89a9-d36904beea12	2026-06-02	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	Major Pharmaceuticals	6be1addd-a811-47fc-8650-6870d661c234	2026-05-26	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	Cardinal Health 107, LLC	71b48f4d-9936-448c-9e3a-33f1182e1039	2026-05-15	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5
Furosemide	FUROSEMIDE	Hospira, Inc.	39fd32f2-6bb7-4a65-d298-e48d26bc80c7	2026-05-13	Warnings, Adverse reactions	Exact identifier unii: 7LXU5N7ZO5

Reported adverse events (FAERS/openFDA)#

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