Why it was recalled
Tablet Separation: Possibility of cracked or split coating on the tablets.
Product description
Perphenazine Tablets, USP, 8 mg, 100-count tablets per bottle, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811, NDC 0603-5092-21.
Lot numbers, UPCs & expiration codes
Lot C1130511A, Exp 5/13
Where it was sold
Nationwide and Puerto Rico
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-010-2013
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Oct 11, 2012
- FDA report date
- Oct 31, 2012
- Quantity
- 2,755 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals
Original FDA data
Every field from FDA enforcement report D-010-2013, exactly as published.
Show all FDA fields
- City
- Huntsville
- State
- AL
- Status
- Terminated
- Country
- United States
- Event ID
- 63502
- Address
- 120 Vintage Dr NE
- Code information
- Lot C1130511A, Exp 5/13
- Postal code
- 35811-8216
- Report date
- Oct 31, 2012
- Product type
- Drugs
- Recall number
- D-010-2013
- Classification
- Class II
- Recalling firm
- Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals
- Product quantity
- 2,755 bottles
- Termination date
- Dec 9, 2013
- Reason for recall
- Tablet Separation: Possibility of cracked or split coating on the tablets.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Perphenazine Tablets, USP, 8 mg, 100-count tablets per bottle, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811, NDC 0603-5092-21.
- Distribution pattern
- Nationwide and Puerto Rico
- Recall initiation date
- Oct 11, 2012
- Initial firm notification
- Letter
- Center classification date
- Oct 22, 2012