FDA Import Refusal 799-0956734-2/10002/1 — Sanofi-Aventis Deutschland GmbH

Sanofi-Aventis Deutschland GmbH — FEI 3003195501

The FDA refused shipment 799-0956734-2/10002/1 from Sanofi-Aventis Deutschland GmbH (Germany) on Dec 5, 2025. The refused product falls under Drugs and Biologics — DUPILUMAB. Cited charge: 75 This firm has 5 or more other import refusals on record.

Refusal details

Date
Dec 5, 2025
Country
Germany
Product Category
Drugs and Biologics
Product Code
58ACK02 DUPILUMAB
Charges
75

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.