NDC 71785-1007-01 - VENLAFAXINE 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

71785-1007

Requested NDC

71785-1007-01

Package NDCs from labels

71785-1007-0, 71785-1007-1, 71785-1007-2, 71785-1007-3, 71785-1007-01

Manufacturer

Annora Pharma Private Limited

Effective date

2020-11-18

Current FDA listing

Not matched in FDA.report NDC product tables