Recalls / Active ingredient / Tizanidine Hydrochloride

Tizanidine Hydrochloride

8 FDA drug recalls involving the active ingredient “Tizanidine Hydrochloride”.

Date	Class	Product	Firm
2024-01-02	Class II	Tizanidine Tablets, USP 4mg, 150-count bottle, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam	Dr. Reddy's Laboratories, Inc.
2023-06-26	Class II	Tizanidine Hydrochloride Tablet 4mg, packaged in a) 20 count-bottles (NDC 68788-7781-2), b)30-count bottles (N	Preferred Pharmaceuticals, Inc.
2023-06-23	Class II	Tizanidine Tablets, USP, 4 mg, 100 Tablets (10 tablets x 10 unit dose blister packs) per carton, Rx Only, Pack	Amerisource Health Services LLC
2023-06-21	Class II	Tizanidine Tablets USP, 4 mg, 1000-Count bottle, Rx Only, Manufactured by Dr. Reddy's Laboratories Limited Sri	Dr Reddy's Laboratories Limited
2021-07-19	Class II	Tizanidine HCl Tablets, USP 4 mg, 150-count bottles, Rx only, Mfd By: Dr. Reddy's Laboratories limited, Srikak	Dr. Reddy's Laboratories, Inc.
2020-11-24	Class II	Tizanidine Tablets, USP 4mg, Rx Only, 150 Tablets per Bottle, Manufactured by Alkem Laboratories Ltd, Mumbai -	Ascend Laboratories LLC
2018-09-04	Class II	Tizanidine HCl Tablets, USP 2mg, 150-count bottles, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited Srilaku	Dr. Reddy's Laboratories, Inc.
2013-03-19	Class III	Tizanidine Tablets USP, 4 mg, 150-count tablets per bottle, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited	Dr. Reddy'S Laboratories