NDC 70518-4672-01 - FENOFIBRATE

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

70518-4672

Requested NDC

70518-4672-01

Package NDCs from labels

70518-4672-1, 70518-4672-0, 70518-4672-01

Manufacturer

REMEDYREPACK INC.

Effective date

2026-06-01

Current FDA listing

Not matched in FDA.report NDC product tables