NDC 70518-3504-01 - Glyburide

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: 70518-3504
Requested NDC: 70518-3504-01
Package NDCs from labels: 70518-3504-0, 70518-3504-1, 70518-3504-01
Manufacturer: REMEDYREPACK INC.
Effective date: 2026-05-15
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
GLYBURIDE TABLETS, USP For Oral Use 1.25, 2.5, and 5 mg	REMEDYREPACK INC.	2026-05-15	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70518-3504-0	Glyburide	30 in 1 BLISTER PACK	TABLET	30		8
70518-3504-1	Glyburide	30 in 1 BLISTER PACK	TABLET	30		8

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70518-3504	GLYBURIDE TABLET [REMEDYREPACK INC.]	4	Current NDC, Legacy NDC, 2 package rows	20240213_e23b9a3b-0184-4d1c-8e2c-668697a6da87.zip

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 · 61 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Glyburide	GLYBURIDE	Proficient Rx LP	240c3ac6-9aab-4185-994e-a0254e3aeb61	2019-11-01	Adverse reactions	Exact identifier rxcui: 310537 unii: SX6K58TVWC

Reported adverse events (FAERS/openFDA)#

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