Sertraline Hydrochloride Tablets Usp, 100 Mg, 90 Tablets Bottles, Rx Only, Manufactured By: Lupin Pharmaceuticals, Inc., Naples, Fl 34108, Ndc 68180-353-09.
Sertraline Recall Summary Lupin Pharmaceuticals is recalling 90-tablet bottles of Sertraline Hydrochloride 100 mg tablets nationwide because the container seals are not adhering properly to the bottles. This recall affects the product with NDC number 68180-353-09 and was distributed across all U.S. states and Washington, D.C.
- Recalling firm
- Lupin Pharmaceuticals Inc.
- Product
- Sertraline Hydrochloride Tablets USP, 100 mg, 90 Tablets bottles, Rx Only, Manufactured by: Lupin Pharmaceuticals, Inc., Naples, FL 34108, NDC 68180-353-09.
- Reason
- Defective container - seal not adhering to bottles
- Classification
- Class I
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2025-11-05
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Nationwide.
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/c1a1b58c-75b6-4394-8e12-3bfe533239ab