Microgestin 24 Fe
These highlights do not include all the information needed to use Microgestin 24 Fe safely and effectively. See full prescribing information for Microgestin 24 FeMicrogestin 24 Fe (norethindrone acetate and ethinyl estradiol tablets and ferrous fumarate tablets) for Oral UseInitial U.S. Approval:1968
Approved
Approval ID
77b9fd75-25cd-4fbc-ab32-f3857d7e2b08
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 12, 2020
Manufacturers
FDA
Mayne Pharma Inc.
DUNS: 867220261
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Norethindrone acetate/Ethinyl Estradiol and Ferrous Fumarate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code51862-648
Application NumberANDA202994
Product Classification
M
Marketing Category
C73584
G
Generic Name
Norethindrone acetate/Ethinyl Estradiol and Ferrous Fumarate
Product Specifications
Effective DateOctober 12, 2020
FDA Product Classification