NEOPHARMA SA DE CV
⚠️ High Risk
FEI: 3021937300 • Vallejo • MEXICO
FEI Number
3021937300
Location
Vallejo
Country
MEXICOAddress
Boulevard Of The Railwa, , Vallejo, , Mexico
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).
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/18/2025 | 66JDA01LEVOTHYROXINE SODIUM (THYROID HORMONE) | Division of Southeast Imports (DSEI) | |
| 12/18/2025 | 62ODA09TELMISARTAN (ANTI-HYPERTENSIVE - PART II) | Division of Southeast Imports (DSEI) | |
| 12/18/2025 | 64BDA25HYDROCHLOROTHIAZIDE (DIURETIC) | Division of Southeast Imports (DSEI) | |
| 5/28/2025 | 66SCB49PENTOXIFYLLINE (VASODILATOR) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 6/10/2024 | 61WCY99A-FUNGAL N.E.C. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 3/13/2024 | 66VDY99MISCELLANEOUS PATENT MEDICINES, ETC. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is NEOPHARMA SA DE CV's FDA import refusal history?
NEOPHARMA SA DE CV (FEI: 3021937300) has 6 FDA import refusal record(s) in our database, spanning from 3/13/2024 to 12/18/2025.
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. NEOPHARMA SA DE CV's FEI number is 3021937300.
What types of violations has NEOPHARMA SA DE CV received?
NEOPHARMA SA DE CV 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 NEOPHARMA SA DE CV come from?
All FDA import refusal data for NEOPHARMA SA DE CV 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.