Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Carbamazepine 200 mg Tablets Recalled by RemedyRepack Inc. Due to FAILED DISSOLUTION SPECIFICATION: Low out-of-specification (OOS) dissolution results...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact RemedyRepack Inc. directly.
Affected Products
Carbamazepine 200 mg Tablets, 100-unit dose tablets per box, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-2489-00 for box; 70518-2489-01 per unit dose.
Quantity: 498 tablets
Why Was This Recalled?
FAILED DISSOLUTION SPECIFICATION: Low out-of-specification (OOS) dissolution results obtained during routine stability testing.
Where Was This Sold?
This product was distributed to 1 state: MN
About RemedyRepack Inc.
RemedyRepack Inc. has 60 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report