NDC 69844-071 - HYDROXYZINE 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

69844-071

Package NDCs from labels

69844-071-01, 69844-071-02, 69844-071-03

Manufacturer

Graviti Pharmaceuticals Private Limited

Effective date

2024-10-19

Current FDA listing

Not matched in FDA.report NDC product tables