Recalls / Active ingredient / Clobetasol Propionate

Clobetasol Propionate

7 FDA drug recalls involving the active ingredient “Clobetasol Propionate” — 1 Class I.

Date	Class	Product	Firm
2023-01-20	Class III	Clobetasol propionate Cream USP, 0.05%, 45 g tube, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc. Balt	Lupin Pharmaceuticals Inc.
2021-12-15	Class I	Clobetasol Propionate Ointment USP, 0.05%, 60g tubes, Rx only, Mfd. by: Taro Pharmaceutical Industries Ltd., H	Taro Pharmaceuticals U.S.A., Inc.
2019-11-15	Class III	Clobetasol Propionate Foam (Emulsion Formulation), 0.05% a) 50 g pack (NDC 68462-625-27) and b) 100 g pack (ND	Glenmark Pharmaceuticals Inc., USA
2019-11-15	Class III	Clobetasol Propionate Foam, 0.05%, a) 50 g pack (NDC 68462-608-27) and b) 100 g pack (NDC 68462-608-94), Rx on	Glenmark Pharmaceuticals Inc., USA
2019-01-11	Class III	Clobetasol Propionate Topical Solution USP, 0.05% w/w, 50 mL bottle, Manufactured for: Macleods Pharma USA, In	Oxalis Labs
2017-12-21	Class III	Clobetasol Propionate Cream USP, 0.05% 60 g tube, Rx only Mfd. by: Taro Pharmaceutical Industries Ltd., Haifa	Taro Pharmaceuticals U.S.A., Inc.
2017-06-02	Class III	G & W Clobetasol Propionate Ointment 0.05%, packaged in a) 15 g tube (NDC 0713-0656-15), b) 30 g tube (NDC 071	G & W Laboratories, Inc.