Neuland Laboratories Limited
⚠️ Moderate Risk
FEI: 3003448273 • Hyderabad • INDIA
FEI Number
3003448273
Location
Hyderabad
Country
INDIAAddress
Flat No. 204 2nd Fl Meridian Plaza, , Hyderabad, , India
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).
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/27/2011 | 63BIY02ALBUTEROL SULFATE (BRONCHODILATOR) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 8/19/2009 | 61ECR11SALMETEROL XINAFOATE (ANTI-ASTHMATIC) | New Orleans District Office (NOL-DO) | |
| 9/20/2005 | 61FCS54CIPROFLOXACIN (ANTI-BACTERIAL PART I) (NOT ANTIBIOTIC) | 75UNAPPROVED | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Neuland Laboratories Limited's FDA import refusal history?
Neuland Laboratories Limited (FEI: 3003448273) has 3 FDA import refusal record(s) in our database, spanning from 9/20/2005 to 12/27/2011.
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. Neuland Laboratories Limited's FEI number is 3003448273.
What types of violations has Neuland Laboratories Limited received?
Neuland Laboratories Limited has been cited for 2 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 Neuland Laboratories Limited come from?
All FDA import refusal data for Neuland Laboratories 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.