NEIMETH INT'L PHARMACEUTICAL
⚠️ High Risk
FEI: 3016551803 • Lagos, Lagos • NIGERIA
FEI Number
3016551803
Location
Lagos, Lagos
Country
NIGERIAAddress
Akanni Close St., Doherty, Lagos, Lagos, Nigeria
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/12/2025 | 60ZDA30PRAZIQUANTEL/PYRANTEL PAMOATE COMBINATION (ANTIPARASITIC) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 11/22/2024 | 60WCA31PYRANTEL PAMOATE (ANTHELMINTIC) | 3280FRNMFGREG | Division of West Coast Imports (DWCI) |
| 2/15/2024 | 60WDY31PYRANTEL PAMOATE (ANTHELMINTIC) | 75UNAPPROVED | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is NEIMETH INT'L PHARMACEUTICAL's FDA import refusal history?
NEIMETH INT'L PHARMACEUTICAL (FEI: 3016551803) has 3 FDA import refusal record(s) in our database, spanning from 2/15/2024 to 11/12/2025.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. NEIMETH INT'L PHARMACEUTICAL's FEI number is 3016551803.
What types of violations has NEIMETH INT'L PHARMACEUTICAL received?
NEIMETH INT'L PHARMACEUTICAL has been cited for 2 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about NEIMETH INT'L PHARMACEUTICAL come from?
All FDA import refusal data for NEIMETH INT'L PHARMACEUTICAL is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.