Class III

Drug Recall: Xelpros (latanoprost ophthalmic emulsion) 0.005%, 125mcg/2.5mL, 2.5 mL bottle, Rx only, Manufactured by: Sun Pharmaceutical Ind. Ltd., India., NDC 47335-317-90

SUN PHARMACEUTICAL INDUSTRIES INC · April 22, 2024

Reason for Recall

Failed Release Testing: Out of specification for particulate matter test.

Distribution

TX, PA

States Affected

PA, TX

Quantity Affected

35,069 bottles

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0502-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.