FDA.reportPublic FDA data

NDC 0093-3634 - Vestura

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
0093-3634
Package NDCs from labels
0093-3634-11
Manufacturer
Teva Pharmaceuticals USA, Inc.
Effective date
2023-08-22
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Vestura - Teva Pharmaceuticals USA, Inc.Teva Pharmaceuticals USA, Inc.2023-08-22HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0093-3634-11Vestura24 in 1 BLISTER PACKTABLET243 mg5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0093-3634VESTURA (DROSPIRENONE AND ETHINYL ESTRADIOL) KIT [TEVA PHARMACEUTICALS USA, INC.]4Unmatched20241108_ef288db4-abf9-4634-84e1-7925a81dcb67.zip