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Ferring Pharmaceuticals Inc

⚠️ High Risk

FEI: 1000119907 • Parsippany, NJ • UNITED STATES

FEI

FEI Number

1000119907

📍

Location

Parsippany, NJ

🇺🇸
🏢

Address

100 Interpace Pkwy, , Parsippany, NJ, United States

High Risk

FDA Import Risk Assessment

56.4
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

10
Total Refusals
5
Unique Violations
8/14/2025
Latest Refusal
7/25/2006
Earliest Refusal

Score Breakdown

Violation Severity
72.0×40%
Refusal Volume
38.6×30%
Recency
77.7×20%
Frequency
5.2×10%
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

757×

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).

1183×

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).

1792×

AGR RX

The article appears to be a prescription drug manufactured in the U.S. and offered for import by other than the manufacturer and reimportation does not appear to have been authorized by the Secretary for use in a medical emergency.

32802×

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.

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

Refusal History

DateProductViolationsDivision
8/14/2025
65JDA31PROGESTERONE (PROGESTIN)
75UNAPPROVED
Division of Southeast Imports (DSEI)
2/14/2022
64MDY05MENOTROPINS (GONAD-STIMULATING PRINCIPLE)
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/16/2019
66YCP99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/16/2019
66YCZ99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C.
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Division of Southeast Imports (DSEI)
6/28/2018
64MDY05MENOTROPINS (GONAD-STIMULATING PRINCIPLE)
118NOT LISTED
75UNAPPROVED
Division of Northern Border Imports (DNBI)
6/21/2018
87MOZACID, HYALURONIC, INTRAARTICULAR
237NO PMA
Division of Northeast Imports (DNEI)
7/20/2016
61QDH03DESMOPRESSIN ACETATE (ANTI-DIURETIC)
179AGR RX
New Orleans District Office (NOL-DO)
3/11/2013
64MDK12MENOTROPINS (GONAD-STIMULATING PRINCIPLE)
75UNAPPROVED
New Orleans District Office (NOL-DO)
2/6/2007
64MCL10UROFOLLITROPIN (GONAD-STIMULATING PRINCIPLE)
75UNAPPROVED
New Orleans District Office (NOL-DO)
7/25/2006
64MCP12MENOTROPINS (GONAD-STIMULATING PRINCIPLE)
179AGR RX
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Ferring Pharmaceuticals Inc's FDA import refusal history?

Ferring Pharmaceuticals Inc (FEI: 1000119907) has 10 FDA import refusal record(s) in our database, spanning from 7/25/2006 to 8/14/2025.

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. Ferring Pharmaceuticals Inc's FEI number is 1000119907.

What types of violations has Ferring Pharmaceuticals Inc received?

Ferring Pharmaceuticals Inc has been cited for 5 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 Ferring Pharmaceuticals Inc come from?

All FDA import refusal data for Ferring Pharmaceuticals Inc 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.