Lloyd Laboratories Inc.
⚠️ High Risk
FEI: 3008094605 • Bulacan, Central Luzon • PHILIPPINES
FEI Number
3008094605
Location
Bulacan, Central Luzon
Country
PHILIPPINESAddress
10 Lloyd Avenue, First Bulacam, , Bulacan, Central Luzon, Philippines
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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).
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).
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
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.
RX LEGEND
The article appears to be a prescription drug without a prescription drug legend as required by Section 503(b)(4).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/10/2025 | 62OCA41LOSARTAN POTASSIUM (ANTI-HYPERTENSIVE - PART II) | Division of Southeast Imports (DSEI) | |
| 7/3/2012 | 66VBH99MISCELLANEOUS PATENT MEDICINES, ETC. | San Francisco District Office (SAN-DO) | |
| 4/30/2012 | 61GCA57SULFAMETHOXAZOLE (ANTI-BACTERIAL) (NOT ANTIBIOTIC) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 4/30/2012 | 66SCA27NIFEDIPINE (VASODILATOR) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 4/30/2012 | 66SCA27NIFEDIPINE (VASODILATOR) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 8/31/2010 | 66YAH99EXHIBITS - OTHER DRUG RELATED ITEMS N.E.C. | Los Angeles District Office (LOS-DO) | |
| 8/27/2010 | 66FDB99SUPPRESSANT N.E.C. | 75UNAPPROVED | San Francisco District Office (SAN-DO) |
| 10/27/2008 | 60LAY01ACETAMINOPHEN (ANALGESIC) | San Francisco District Office (SAN-DO) | |
| 10/27/2008 | 56CCC99CEPHALOSPORIN N.E.C. | San Francisco District Office (SAN-DO) | |
| 6/21/2006 | 64LCA56PREDNISONE (GLUCOCORTICOID) | 75UNAPPROVED | Seattle District Office (SEA-DO) |
Frequently Asked Questions
What is Lloyd Laboratories Inc.'s FDA import refusal history?
Lloyd Laboratories Inc. (FEI: 3008094605) has 10 FDA import refusal record(s) in our database, spanning from 6/21/2006 to 11/10/2025.
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. Lloyd Laboratories Inc.'s FEI number is 3008094605.
What types of violations has Lloyd Laboratories Inc. received?
Lloyd Laboratories 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 Lloyd Laboratories Inc. come from?
All FDA import refusal data for Lloyd Laboratories 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.