Class III · Low riskOngoing Initiated Jan 25, 2024 (3 years ago)
Nortrel (norethindrone and ethinyl estradiol tablets USP) 0.5/35, packaged in cartons…
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.
What was recalled
Nortrel (norethindrone and ethinyl estradiol tablets USP) 0.5/35, packaged in cartons, each carton contains 3 blister cards, each card contains 28 tablets, Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC 0555-9008-67
Recalling firm
Teva Pharmaceuticals USA, Inc
NDC code
0555-9008-67
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0321-2024
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.