FDA Drug Recalls

Recalls / Brands / Nortrel 7/7/7

Nortrel 7/7/7

1 FDA drug recall involving brand “Nortrel 7/7/7.

DateClassProductFirm
2024-01-25Class IIINortrel 7/7/7 (norethindrone and ethinyl estradiol tablets USP- triphasic regimen), packaged in cartons, each Teva Pharmaceuticals USA, Inc