NDC 0781-4075-52 - Drospirenone/Ethinyl Estradiol/Levomefolate Calcium and Levomefolate Calcium

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

0781-4075

Requested NDC

0781-4075-52

Package NDCs from labels

0781-4075-52, 0781-4075-15

Manufacturer

Sandoz Inc | Bayer HealthCare Pharmaceuticals Inc. | Bayer Weimar GmbH und Co. KG | Bayer AG | Sharp Corporation

Effective date

2023-05-19

Current FDA listing

Not matched in FDA.report NDC product tables