Alprazolam Tab, USP 0.5mg, (CIV), packaged in: a) 30-count bottle (NDC 68788-7595-3), b) 60-count bottle (NDC 68788-7595-6), c) 90-count bottle (NDC 68788-7595-9); Rx Only, Preferred Pharmaceuticals, Inc. Manufactured by: Breckenridge Pharmaceuticals, Inc., Boca Raton, FL.
Reported: April 12, 2023 Initiated: March 27, 2023 #D-0505-2023
Product Description
Alprazolam Tab, USP 0.5mg, (CIV), packaged in: a) 30-count bottle (NDC 68788-7595-3), b) 60-count bottle (NDC 68788-7595-6), c) 90-count bottle (NDC 68788-7595-9); Rx Only, Preferred Pharmaceuticals, Inc. Manufactured by: Breckenridge Pharmaceuticals, Inc., Boca Raton, FL.
Reason for Recall
CGMP Deviations: Downstream recall from Breckenridge Pharmaceuticals, Inc due to potential risk of Cross Contamination.
Details
- Recalling Firm
- Preferred Pharmaceuticals, Inc.
- Units Affected
- 320 x 30-count; 46 x 60-count; 10 x 90-count bottles
- Distribution
- Nationwide in the USA
- Location
- Anaheim, CA
Frequently Asked Questions
What product was recalled? ▼
Alprazolam Tab, USP 0.5mg, (CIV), packaged in: a) 30-count bottle (NDC 68788-7595-3), b) 60-count bottle (NDC 68788-7595-6), c) 90-count bottle (NDC 68788-7595-9); Rx Only, Preferred Pharmaceuticals, Inc. Manufactured by: Breckenridge Pharmaceuticals, Inc., Boca Raton, FL.. Recalled by Preferred Pharmaceuticals, Inc.. Units affected: 320 x 30-count; 46 x 60-count; 10 x 90-count bottles.
Why was this product recalled? ▼
CGMP Deviations: Downstream recall from Breckenridge Pharmaceuticals, Inc due to potential risk of Cross Contamination.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 12, 2023. Severity: Moderate. Recall number: D-0505-2023.
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