Pharmasave #42
⚠️ Moderate Risk
FEI: 3004442339 • Estevan, SK • CANADA
FEI Number
3004442339
Location
Estevan, SK
Country
CANADAAddress
1239 5th St Sk, , Estevan, SK, Canada
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
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 |
|---|---|---|---|
| 3/10/2004 | 63NDB03BETHANECHOL CHLORIDE (CHOLINERGIC) | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
| 3/10/2004 | 61MDF24PHENYTOIN SODIUM (ANTI-CONVULSANT) | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
| 3/10/2004 | 61JDB08ATORVASTATIN CALCIUM (ANTI-CHOLESTEREMIC) | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
| 3/10/2004 | 66JDC01LEVOTHYROXINE SODIUM (THYROID HORMONE) | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
| 3/10/2004 | 62ODB44METOPROLOL TARTRATE (ANTI-HYPERTENSIVE - PART II) | 75UNAPPROVED | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is Pharmasave #42's FDA import refusal history?
Pharmasave #42 (FEI: 3004442339) has 5 FDA import refusal record(s) in our database, spanning from 3/10/2004 to 3/10/2004.
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. Pharmasave #42's FEI number is 3004442339.
What types of violations has Pharmasave #42 received?
Pharmasave #42 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 Pharmasave #42 come from?
All FDA import refusal data for Pharmasave #42 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.