FDA.reportPublic FDA data

NDC 68462-821 - Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate

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
68462-821
Package NDCs from labels
68462-821-40
Manufacturer
Glenmark Pharmaceuticals Inc., USA | Cyndea Pharma SL
Effective date
2026-01-31
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
NORETHINDRONE ACETATE - Glenmark Pharmaceuticals Inc., USA | Cyndea Pharma SLGlenmark Pharmaceuticals Inc., USA | Cyndea Pharma SL2026-01-31HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68462-821-40Norethindrone Acetate and Ethinyl Estradiol and Ferrous Fumarate24 in 1 BLISTER PACKCAPSULE, LIQUID FILLED241 mg3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68462-821NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE KIT [GLENMARK PHARMACEUTICALS INC., USA]2Unmatched20230926_3e608414-5e64-4c69-a9e0-365904cf7df8.zip