FDA Import Refusal AEK-7427560-0/21/1 — Novartis Pharma AG

Novartis Pharma AG — FEI 3009487425

The FDA refused shipment AEK-7427560-0/21/1 from Novartis Pharma AG (Switzerland) on Jun 2, 2020. The refused product falls under Drugs and Biologics — AMLODIPINE BESYLATE (ANTI-HYPERTENSIVE, PART II). Cited charge: 75 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jun 2, 2020
Country
Switzerland
Product Category
Drugs and Biologics
Product Code
62ODY14 AMLODIPINE BESYLATE (ANTI-HYPERTENSIVE, PART II)
Charges
75

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