Glenmark Pharmaceuticals Inc., USA: Aspirin and Extended-Release Dipyridamole Capsules, 25mg/200 mg, 60-count bottle, Rx Only, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, P

Is my product affected?

Aspirin and Extended-Release Dipyridamole Capsules, 25mg/200 mg, 60-count bottle, Rx Only, Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, Product of India, NDC 68462-405-60.

• Brand ASPRIN AND EXTENDED-RELEASE DIPYRIDAMOLE

Check against the official notice below — it lists the full affected range.

What happened

Glenmark Pharmaceuticals Inc., USA is recalling Aspirin and Extended-Release Dipyridamole Capsules (25mg/200mg) in 60-count bottles distributed nationwide. The recall affects 168,936 bottles across multiple lots with expiration dates ranging from August 2022 through December 2023 due to capsule breakage that failed to meet tablet/capsule specifications.

The source does not specify a remedy for consumers who have purchased this product.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

Failed Tablet/Capsule Specification : Capsule breakage

Details from the source

Reason for recall: Failed Tablet/Capsule Specification : Capsule breakage Distribution: USA Nationwide Quantity: 168936 bottles Lot/code info: Lot#: 17201639, Exp 08/2022; 17201759, Exp 09/2022; 17202067, Exp 10/2022; 17210696, Exp 02/2023; 17210092, Exp 11/2022; 17210145, Exp 12/2022; 17210732, Exp 02/2023; 17211062, Exp 04/2023; 17211441, Exp 05/2023; 17211670, Exp 06/2023; 17211810, Exp 07/2023; 17211862, 17212020, 17212068, Exp 08/2023; 17212438, Exp 10/2023; 17220172, 17220251, Exp 12/2023.

Source

Official record: FDA (Drug enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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