Why it was recalled
Failed Dissolution Specifications; the product is dissolving faster than the specified limits.
Product description
buPROPion Hydrochloride Extended-release Tablets USP (XL) Once-Daily, 150 mg, 100 Tablets (10 x 10) per carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC: 60687-782-01.
Lot numbers, UPCs & expiration codes
Lot 1017343, Exp. 12/31/2025
Where it was sold
Nationwide in the USA
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0590-2024
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- Jun 24, 2024
- FDA report date
- Jul 17, 2024
- Quantity
- 2,484 cartons
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Amerisource Health Services LLC
Original FDA data
Every field from FDA enforcement report D-0590-2024, exactly as published.
Show all FDA fields
- City
- Columbus
- State
- OH
- Status
- Ongoing
- Country
- United States
- Event ID
- 94891
- Address
- 2550 John Glenn Ave Ste A
- Code information
- Lot 1017343, Exp. 12/31/2025
- Postal code
- 43217-1188
- Report date
- Jul 17, 2024
- Product type
- Drugs
- Recall number
- D-0590-2024
- Classification
- Class II
- Recalling firm
- Amerisource Health Services LLC
- Product quantity
- 2,484 cartons
- Reason for recall
- Failed Dissolution Specifications; the product is dissolving faster than the specified limits.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- buPROPion Hydrochloride Extended-release Tablets USP (XL) Once-Daily, 150 mg, 100 Tablets (10 x 10) per carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC: 60687-782-01.
- Distribution pattern
- Nationwide in the USA
- Recall initiation date
- Jun 24, 2024
- Initial firm notification
- Letter
- Center classification date
- Jul 8, 2024