US Drug Recall Register
Class III · Low risk Ongoing 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.

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