Telmisartan Tablets, USP 20 mg, 30-count bottles, Rx only, Manufactured by: Alembic…

Class I — High risk. Reasonable probability of serious harm or death.

Recalling firm

Alembic Pharmaceuticals Limited

NDC code

62332-087-30

Origin

N/A, India

Initiated by

Voluntary: Firm initiated

FDA recall number

D-0326-2021

Other Telmisartan recalls

See all

Class II · Moderate risk Terminated Feb 9, 2024

Telmisartan Tablets, USP 40mg, Rx Only, 30 Tablets per bottle, Manufactured by: Micro Labs Limited Goa-403 722, INDIA…

Reason Failed Stability Specifications: Out of specification for blend uniformity.

Micro Labs Limited NDC 42571-227-30 D-0388-2024

Class II · Moderate risk Terminated Jun 29, 2022

Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/12.5 mg, 30 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceuticals…

Reason Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the…

Glenmark Pharmaceuticals Inc., USA NDC 68462-841-13 D-1306-2022

Class II · Moderate risk Terminated Jun 29, 2022

Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/25 mg, 30 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceuticals…

Reason Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the…

Glenmark Pharmaceuticals Inc., USA NDC 68462-842-13 D-1305-2022

Class III · Low risk Terminated Dec 1, 2021

Telmisartan and Hydrochlorothiazide Tablets, USP, 40 mg/12.5 mg, 30 count bottles, Rx only, Manufactured by: Torrent…

Reason Superpotent; Hydrochlorothiazide

Torrent Pharma Inc. D-0285-2022

Class II · Moderate risk Terminated May 4, 2021

Micardis Tablets, (telmisartan Tablets) 80 mg, 30 ct. per folding cartons, Rx only, NDC 0597-0041-37), Distributed by: Boehringer…

Reason Subpotent Drug

Boehringer Ingelheim Pharmaceuticals, Inc. NDC 0597-0041-37 D-0600-2021