Lannett Company Inc. — FDA Class III (D-0533-2026)

Lannett Company Inc. is recalling 44,865 bottles of a human prescription drug due to cross contamination. This recall is classified as a Class II recall. The affected products are identified by NDC numbers 0527-1231 and 0527-1301.

• •Lannett Company Inc. is recalling 44,865 bottles of a human prescription drug.
• •The recall is due to cross contamination with another product.
• •Affected products have NDC numbers 0527-1231 and 0527-1301.
• •Consumers should check their medicine cabinets for these recalled products.

Consumers with the recalled products should stop using them and contact Lannett Company Inc. for further instructions. The recall affects 44,865 bottles.