PlainRecalls
FDA Drug Low Class III Terminated

Levonorgestrel and Ethinyl Estradiol Tablets, USP 0.15 mg/0.03 mg, Rx Only, 3 extended-cycle blister packs containing 91 tablets each, Made in India, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A., NDC 0378-7281-53.

Reported: October 24, 2018 Initiated: August 27, 2018 #D-0025-2019

Product Description

Levonorgestrel and Ethinyl Estradiol Tablets, USP 0.15 mg/0.03 mg, Rx Only, 3 extended-cycle blister packs containing 91 tablets each, Made in India, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A., NDC 0378-7281-53.

Reason for Recall

Labeling: Not Elsewhere Classified-Incorrect NDC and product name identified on blister packs.

Details

Units Affected
5,790 cartons (526,890 tablets)
Distribution
Product was distributed throughout the United States.
Location
Morgantown, WV

Frequently Asked Questions

What product was recalled?
Levonorgestrel and Ethinyl Estradiol Tablets, USP 0.15 mg/0.03 mg, Rx Only, 3 extended-cycle blister packs containing 91 tablets each, Made in India, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A., NDC 0378-7281-53.. Recalled by Mylan Pharmaceuticals Inc.. Units affected: 5,790 cartons (526,890 tablets).
Why was this product recalled?
Labeling: Not Elsewhere Classified-Incorrect NDC and product name identified on blister packs.
Which agency issued this recall?
This recall was issued by the FDA Drug on October 24, 2018. Severity: Low. Recall number: D-0025-2019.