Recalls / Active ingredient / Indomethacin

Indomethacin

7 FDA drug recalls involving the active ingredient “Indomethacin”.

Date	Class	Product	Firm
2025-05-15	Class II	Indomethacin Extended-Release Capsules, USP, 75 mg, 30 capsules (3 x 10 blister cards) per carton, Rx Only, Di	Amerisource Health Services LLC
2025-05-09	Class II	Indomethacin Extended-Release Capsules USP, 75 mg, 100-count bottle, Rx only, Mfd. By: KVK-Tech, Inc., Newtown	KVK Tech, Inc.
2025-03-13	Class II	Indomethacin Extended-Release Capsules, 75mg, 60-count bottles, Manufactured by: Glenmark Pharmaceuticals Limi	Glenmark Pharmaceuticals Inc., USA
2024-07-31	Class II	Indomethacin Extended-Release Capsules, USP, 75 mg, packaged in a) 60-count bottle (NDC 68462-325-60) and b)	Glenmark Pharmaceuticals Inc., USA
2023-11-07	Class II	Indomethacin 25mg Capsules, USP, 100-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd. Col	Glenmark Pharmaceuticals Inc., USA
2018-07-18	Class II	Indomethacin Capsules, USP, 50 mg, 100-count bottles, Rx only, Manufactured for: Camber Pharmaceuticals, Inc.,	Hetero Labs, Ltd. - Unit III
2018-03-19	Class III	Indomethacin Capsules USP, 50 mg, 100-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., C	Glenmark Pharmaceuticals Inc., USA