Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count cartons (NDC 0113-0847-39), and b) 45-count cartons (NDC 0113-0847-95), Distributed by: Perrigo, Allegan, MI 49010.
Reported: July 19, 2023 Initiated: February 9, 2023 #D-0908-2023
Product Description
Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count cartons (NDC 0113-0847-39), and b) 45-count cartons (NDC 0113-0847-95), Distributed by: Perrigo, Allegan, MI 49010.
Reason for Recall
Failed Impurities/Degradation Specifications
Details
- Recalling Firm
- L. Perrigo Company
- Units Affected
- 32,376 cartons
- Distribution
- Nationwide within the USA
- Location
- Allegan, MI
Frequently Asked Questions
What product was recalled? ▼
Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count cartons (NDC 0113-0847-39), and b) 45-count cartons (NDC 0113-0847-95), Distributed by: Perrigo, Allegan, MI 49010.. Recalled by L. Perrigo Company. Units affected: 32,376 cartons.
Why was this product recalled? ▼
Failed Impurities/Degradation Specifications
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 19, 2023. Severity: Moderate. Recall number: D-0908-2023.
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