Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer, Inc.
⚠️ Moderate Risk
FEI: 1310337 • Rouses Point, NY • UNITED STATES
FEI Number
1310337
Location
Rouses Point, NY
Country
UNITED STATESAddress
64 Maple St, , Rouses Point, NY, United States
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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
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.
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).
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/24/2021 | 66MCA86LORAZEPAM (TRANQUILIZER) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 7/12/2007 | 64TCA01AZATHIOPRINE (IMMUNOSUPPRESSIVE) | 179AGR RX | Division of West Coast Imports (DWCI) |
| 5/10/2007 | 61NCF80VENLAFAXINE HYDROCHLORIDE (ANTI-DEPRESSANT) | 179AGR RX | New Orleans District Office (NOL-DO) |
| 12/5/2003 | 62GAA41IBUPROFEN (ANTI-INFLAMMATORY) | 118NOT LISTED | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer, Inc.'s FDA import refusal history?
Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer, Inc. (FEI: 1310337) has 4 FDA import refusal record(s) in our database, spanning from 12/5/2003 to 3/24/2021.
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. Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer, Inc.'s FEI number is 1310337.
What types of violations has Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer, Inc. received?
Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer, Inc. has been cited for 3 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 Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer, Inc. come from?
All FDA import refusal data for Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer, 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.