Aripiprazole Tablets, USP, 10 mg, 30-count bottles, Rx only, Manufactured by: Alken Laboratories Ltd., INDIA; Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054. NDC: 67877-432-03
Reported: September 24, 2025 Initiated: August 28, 2025 #D-0645-2025
Product Description
Aripiprazole Tablets, USP, 10 mg, 30-count bottles, Rx only, Manufactured by: Alken Laboratories Ltd., INDIA; Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054. NDC: 67877-432-03
Reason for Recall
Superpotent drug
Details
- Recalling Firm
- Ascend Laboratories, LLC
- Units Affected
- 2,256 bottles
- Distribution
- Nationwide in the USA.
- Location
- Bedminster, NJ
Frequently Asked Questions
What product was recalled? ▼
Aripiprazole Tablets, USP, 10 mg, 30-count bottles, Rx only, Manufactured by: Alken Laboratories Ltd., INDIA; Distributed by: Ascend Laboratories, LLC, Parsippany, NJ 07054. NDC: 67877-432-03. Recalled by Ascend Laboratories, LLC. Units affected: 2,256 bottles.
Why was this product recalled? ▼
Superpotent drug
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on September 24, 2025. Severity: Moderate. Recall number: D-0645-2025.
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