Recalls / Active ingredient / Pseudoephedrine Sulfate
Pseudoephedrine Sulfate
3 FDA drug recalls involving the active ingredient “Pseudoephedrine Sulfate”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2021-10-12 | Class III | AllerClear D-24 hr, (Loratadine and Pseudoephedrine Sulfate, Extended-Release Tablets, USP 10/240mg), 15-count | SUN PHARMACEUTICAL INDUSTRIES INC |
| 2021-10-12 | Class III | Loratadine-D Extended-Release Tablets (Loratadine and Pseudoephedrine Sulfate, Extended-Release Tablets, USP 1 | SUN PHARMACEUTICAL INDUSTRIES INC |
| 2014-02-07 | Class II | Non-Drowsy 24 Hour Formula Allergy Relief and Nasal Decongestant, Pseudoephedrine Sulfate, USP 240 mg , Lorata | Ohm Laboratories, Inc. |