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.
Reported: July 27, 2022 Initiated: June 29, 2022 #D-1282-2022
Product Description
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.
Reason for Recall
Failed Tablet/Capsule Specification : Capsule breakage
Details
- Recalling Firm
- Glenmark Pharmaceuticals Inc., USA
- Units Affected
- 168936 bottles
- Distribution
- USA Nationwide
- Location
- Mahwah, NJ
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Glenmark Pharmaceuticals Inc., USA. Units affected: 168936 bottles.
Why was this product recalled? ▼
Failed Tablet/Capsule Specification : Capsule breakage
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 27, 2022. Severity: Low. Recall number: D-1282-2022.
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