NDC 23155-196-31 - Ondansetron Hydrochloride

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

23155-196

Requested NDC

23155-196-31

Package NDCs from labels

23155-196-31, 23155-196-41, 23155-196-43, 23155-196-42

Manufacturer

Heritage Pharmaceuticals Inc. | Emcure Pharmaceuticals Limited

Effective date

2018-09-28

Current FDA listing

Not matched in FDA.report NDC product tables