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
4bdfc5fa-76c8-4c85-acd0-fb6461c72d7c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Aug 11, 2023
Manufacturers
FDA
RPK Pharmaceuticals, Inc.
DUNS: 147096275
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 Code53002-3567
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