FDAFDA · Food and drugs·Recall number D-0015-2021
Citalopram Oral Solution, USP 20 mg/10 mL, 10 mL unit dose cups, Rx Only, Mfg for: Pharmaceutical Associates, Inc. Greenville, SC 29605 NDC 0121-1696-40
Published October 14, 2020 · Recall initiated: September 9, 2020
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impurities/Degradation Specifications; high out of specification results obtained at the 9 month stability timepoint
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- PAI Holdings, LLC. dba Pharmaceutical Associates Inc
- Distributor
- Nationwide.
- Lot
- Lots: C1EE Exp. 04/2021, BD82 Exp. 11/2020, BD83 Exp. 11/2020, C16D Exp. 02/2021, C563 Exp. 11/2021, C574 Exp. 11/2021
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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