FDA.reportPublic FDA data

NDC 0480-3080 - Budesonide and formoterol fumarate dihydrate

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
0480-3080
Package NDCs from labels
0480-3080-31
Manufacturer
Teva Pharmaceuticals, Inc.
Effective date
2022-11-01
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Budesonide and formoterol fumarate dihydrate - Teva Pharmaceuticals, Inc.Teva Pharmaceuticals, Inc.2022-11-01HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0480-3080-31Budesonide and formoterol fumarate dihydrate1 in 1 CARTONAEROSOL, METERED12
0480-3080-31Budesonide and formoterol fumarate dihydrate1 in 1 POUCHAEROSOL, METERED12