FDA Import Refusal AEK-9041776-5/40003/1 — NEOPHARMA SA DE CV

NEOPHARMA SA DE CV — FEI 3021937300

The FDA refused shipment AEK-9041776-5/40003/1 from NEOPHARMA SA DE CV (Mexico) on Dec 18, 2025. The refused product falls under Drugs and Biologics — TELMISARTAN (ANTI-HYPERTENSIVE - PART II). Cited charges: 118,75 This firm has 5 or more other import refusals on record.