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FDA Import Refusal AEK-3046284-7/101/1 — Wyeth Consumer Healthcare

Wyeth Consumer Healthcare — FEI 3003851828

The FDA refused shipment AEK-3046284-7/101/1 from Wyeth Consumer Healthcare (United States) on Mar 21, 2017. The refused product falls under Drugs and Biologics — AMIODARONE HYDROCHLORIDE (CARDIAC DEPRESSANT (ANTI-ARRHYTHMIC)). Cited charge: 75 This firm has 3 other import refusals on record.

Refusal details

Date
Mar 21, 2017
Country
United States
Product Category
Drugs and Biologics
Product Code
63EDA19 AMIODARONE HYDROCHLORIDE (CARDIAC DEPRESSANT (ANTI-ARRHYTHMIC))
Charges
75

Other import refusals

FDA data resources

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