Microgestin Fe 1.5/30
Microgestin® Fe 1.5/30(Norethindrone Acetate and Ethinyl Estradiol Tablets, USP and Ferrous Fumarate Tablets*)*Ferrous fumarate tablets are not USP for dissolution.
Approved
Approval ID
1587721b-0d71-4fe7-9e34-eac41a115203
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 23, 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 Code51862-870
Application NumberANDA091453
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