Ajanta Pharma USA Inc: Aripiprazole Tablets Usp
Ajanta Pharma USA Inc is recalling Aripiprazole Tablets USP 30 mg (NDC 27241-056-03) distributed nationwide because some bottles were mislabeled and contain Voriconazole 50 mg instead. Aripiprazole is used to treat mental health conditions, while Voriconazole is an antifungal medication, so patients taking the recalled product would be receiving the wrong medication. The affected product was manufactured in India and distributed across all U.S. states and Washington, D.C.
- Recalling firm
- Ajanta Pharma USA Inc
- Product
- Aripiprazole Tablets USP, Rx only, 30 mg, 30 tablets, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India, NDC 27241-056-03.
- Reason
- Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-05-27
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- U.S. Nationwide
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/0af24804-7eeb-4157-8fd3-872c6d37de76