Interthai Pharmaceutical Manufacturing Limited
⚠️ Moderate Risk
FEI: 3003002183 • Chatuchak, Bangkok • THAILAND
FEI Number
3003002183
Location
Chatuchak, Bangkok
Country
THAILANDAddress
Ladyao, 1899; Phahon Yothin Rd (Soi 39); Krung Thep Maha Nakhon, Chatuchak, Bangkok, Thailand
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
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).
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/12/2023 | 62MCY08MENTHOL (ANTI-PRURITIC) | Division of Southeast Imports (DSEI) | |
| 8/24/2021 | 66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC. | Division of Northern Border Imports (DNBI) | |
| 10/28/2011 | 60LAP99ANALGESIC, N.E.C. | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 7/25/2003 | 64LDO08BETAMETHASONE VALERATE (GLUCOCORTICOID) | 75UNAPPROVED | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Interthai Pharmaceutical Manufacturing Limited's FDA import refusal history?
Interthai Pharmaceutical Manufacturing Limited (FEI: 3003002183) has 4 FDA import refusal record(s) in our database, spanning from 7/25/2003 to 6/12/2023.
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. Interthai Pharmaceutical Manufacturing Limited's FEI number is 3003002183.
What types of violations has Interthai Pharmaceutical Manufacturing Limited received?
Interthai Pharmaceutical Manufacturing Limited 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 Interthai Pharmaceutical Manufacturing Limited come from?
All FDA import refusal data for Interthai Pharmaceutical Manufacturing Limited 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.