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HP Halden Pharma AS

⚠️ Moderate Risk

FEI: 3002608066 • Halden, Viken • NORWAY

FEI

FEI Number

3002608066

📍

Location

Halden, Viken

🇳🇴

Country

NORWAY
🏢

Address

Svinesundsveien 80, , Halden, Viken, Norway

Moderate Risk

FDA Import Risk Assessment

43.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
10/31/2012
Latest Refusal
3/11/2003
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
3.1×10%
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

753×

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).

Refusal History

DateProductViolationsDivision
10/31/2012
65QCK64ROPIVACAINE HCL MONOHYDRATE (RELAXANT)
75UNAPPROVED
Chicago District Office (CHI-DO)
9/25/2012
65QCK64ROPIVACAINE HCL MONOHYDRATE (RELAXANT)
75UNAPPROVED
Chicago District Office (CHI-DO)
3/11/2003
66VIP99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New York District Office (NYK-DO)

Frequently Asked Questions

What is HP Halden Pharma AS's FDA import refusal history?

HP Halden Pharma AS (FEI: 3002608066) has 3 FDA import refusal record(s) in our database, spanning from 3/11/2003 to 10/31/2012.

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. HP Halden Pharma AS's FEI number is 3002608066.

What types of violations has HP Halden Pharma AS received?

HP Halden Pharma AS has been cited for 1 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 HP Halden Pharma AS come from?

All FDA import refusal data for HP Halden Pharma AS 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.