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Newport Pharmaceutical

⚠️ Moderate Risk

FEI: 3004464597 • San Jose • COSTA RICA

FEI

FEI Number

3004464597

📍

Location

San Jose

🇨🇷

Country

COSTA RICA
🏢

Address

2nd Avenue S/n, , San Jose, , Costa Rica

Moderate Risk

FDA Import Risk Assessment

33.8
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

2
Total Refusals
2
Unique Violations
7/21/2008
Latest Refusal
4/9/2004
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
4.7×10%
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

752×

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).

4721×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).

Refusal History

DateProductViolationsDivision
7/21/2008
60RDA19SIBUTRAMINE HCL MONOHYDRATE (ANOREXIC)
472NO ENGLISH
75UNAPPROVED
New Orleans District Office (NOL-DO)
4/9/2004
66VCP99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Newport Pharmaceutical's FDA import refusal history?

Newport Pharmaceutical (FEI: 3004464597) has 2 FDA import refusal record(s) in our database, spanning from 4/9/2004 to 7/21/2008.

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. Newport Pharmaceutical's FEI number is 3004464597.

What types of violations has Newport Pharmaceutical received?

Newport 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 Newport Pharmaceutical come from?

All FDA import refusal data for Newport 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.