Mimvey (estradiol and norethindrone acetate tablets USP) 1 mg/0.5 mg, packaged in cartons of 28 Tablets, Rx Only, Manufactured By: Barr Laboratories, Inc., Pomona, NY 10970, Manufactured For: Teva Pharmaceuticals USA Inc. North Wales, PA 19454, NDC 0093-5455-42
Reported: February 9, 2022 Initiated: January 7, 2022 #D-0522-2022
Product Description
Mimvey (estradiol and norethindrone acetate tablets USP) 1 mg/0.5 mg, packaged in cartons of 28 Tablets, Rx Only, Manufactured By: Barr Laboratories, Inc., Pomona, NY 10970, Manufactured For: Teva Pharmaceuticals USA Inc. North Wales, PA 19454, NDC 0093-5455-42
Reason for Recall
Mislabeling
Details
- Recalling Firm
- Teva Pharmaceuticals USA
- Units Affected
- 6430 cartons
- Distribution
- USA Nationwide
- Location
- Parsippany, NJ
Frequently Asked Questions
What product was recalled? ▼
Mimvey (estradiol and norethindrone acetate tablets USP) 1 mg/0.5 mg, packaged in cartons of 28 Tablets, Rx Only, Manufactured By: Barr Laboratories, Inc., Pomona, NY 10970, Manufactured For: Teva Pharmaceuticals USA Inc. North Wales, PA 19454, NDC 0093-5455-42. Recalled by Teva Pharmaceuticals USA. Units affected: 6430 cartons.
Why was this product recalled? ▼
Mislabeling
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 9, 2022. Severity: Low. Recall number: D-0522-2022.
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