Recalls / Active ingredient / Tadalafil

Tadalafil

9 FDA drug recalls involving the active ingredient “Tadalafil”.

Date	Class	Product	Firm
2023-03-23	Class II	Tadalafil Tablets, USP, 20 mg, 7-count bottle, Rx only, Manufactured for: Accord Healthcare, lnc., Durham, NC	Preferred Pharmaceuticals, Inc.
2023-03-16	Class II	Tadalafil Tablets, USP 20 mg, packaged in a) 6-count bottles (NDC 51655-473-87), and b) 15-count bottles (NDC	Northwind Pharmaceuticals LLC
2023-03-16	Class II	Tadalafil Tablets, USP 5 mg, 30-count bottles, Rx Only, Repackaged By: Northwind Pharmaceuticals, Indianapolis	Northwind Pharmaceuticals LLC
2023-02-07	Class II	Tadalafil Tablets, USP, 20 mg, Rx Only, Packaged as: a) 30-count bottle NDC 16729-372-10, UPC 3 16729 37210 7	Accord Healthcare, Inc.
2023-02-07	Class II	Tadalafil Tablets, USP, 5 mg Rx Only, Packaged as: a) 30-count bottle NDC 16729-370-10, UPC 3 16729 37010 3; b	Accord Healthcare, Inc.
2023-02-07	Class II	Tadalafil Tablets, USP, 2.5 mg Rx Only, Packaged as: a) 30-count bottle NDC 16729-369-10, UPC 3 16729 36910 7	Accord Healthcare, Inc.
2023-02-07	Class II	Tadalafil Tablets, USP 10 mg Rx Only, Packaged as: a) 30-count bottle NDC 16729-371-10, UPC 3 16729 37110 0;	Accord Healthcare, Inc.
2021-10-25	Class II	Tadalafil Tablets, USP 5 mg, 30 count bottle, Rx Only, Manufactured for: Northstar Rx LLC Memphis, TN 38141, M	SUN PHARMACEUTICAL INDUSTRIES INC
2021-10-25	Class II	Tadalafil Tablets, USP 20 mg, 30 count bottle, Rx Only, Manufactured for: Northstar Rx LLC Memphis, TN 38141,	SUN PHARMACEUTICAL INDUSTRIES INC