Microgestin Fe 1/20
Microgestin® Fe 1/20(Norethindrone Acetate and Ethinyl Estradiol Tablets, USP and Ferrous Fumarate Tablets*)*Ferrous fumarate tablets are not USP for dissolution.
Approved
Approval ID
5bf28e22-8f58-4166-8a62-2717ecd6a70f
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
NDC Product Code51862-866
Application NumberANDA091454
Marketing CategoryC73584
Route of AdministrationN/A
Effective DateOctober 12, 2020
Generic NameNorethindrone Acetate/Ethinyl Estradiol and Ferrous Fumarate