Prochlorperazine Maleate Tablets
CGMP Deviations
Yes — there is an active recall. 1 ongoing FDA recall mention Prochlorperazine (3 total). Check the affected lots below.
Most common reason: cGMP deviation (1 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Prochlorperazine. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
CGMP Deviations
Subpotent Drug: Out of specification for assay at the 18-month stability timepoint.
Non-Sterility:Microbial growth detected in sub lot of Amikacin Sulfate Injection, USP 1gm/4 mL (250mg/mL) and Prochlorperazine Edisylate Injection, USP 10mg/2mL (5mg/mL) .
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