NDC 68788-7672-01 - Duloxetine

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

68788-7672

Requested NDC

68788-7672-01

Package NDCs from labels

68788-7672-0, 68788-7672-1, 68788-7672-2, 68788-7672-3, 68788-7672-6, 68788-7672-9, 68788-7672-8, 68788-7672-01

Manufacturer

Preferred Pharmaceuticals, Inc.

Effective date

2025-04-04

Current FDA listing

Not matched in FDA.report NDC product tables