AVKARE Fexofenadine Hydrochloride Tablets USP Antihistamine 180 mg, 500 Tablets per bottle, NDC 42291-297-50.
Reported: September 18, 2019 Initiated: August 28, 2019 #D-1875-2019
Product Description
AVKARE Fexofenadine Hydrochloride Tablets USP Antihistamine 180 mg, 500 Tablets per bottle, NDC 42291-297-50.
Reason for Recall
Failed Stability Specifications.
Details
- Recalling Firm
- AVKARE Inc.
- Units Affected
- 5953 bottles
- Distribution
- Nationwide in the U.S.
- Location
- Pulaski, TN
Frequently Asked Questions
What product was recalled? ▼
AVKARE Fexofenadine Hydrochloride Tablets USP Antihistamine 180 mg, 500 Tablets per bottle, NDC 42291-297-50.. Recalled by AVKARE Inc.. Units affected: 5953 bottles.
Why was this product recalled? ▼
Failed Stability Specifications.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on September 18, 2019. Severity: Moderate. Recall number: D-1875-2019.
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