NDC 31722-892-31 - Olmesartan medoxomil, amlodipine and hydrochlorothiazide

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

31722-892

Requested NDC

31722-892-31

Package NDCs from labels

31722-892-30, 31722-892-90, 31722-892-31, 31722-892-32

Manufacturer

Camber Pharmaceuticals, Inc. | Hetero Labs Limited Unit V

Effective date

2026-01-05

Current FDA listing

Not matched in FDA.report NDC product tables