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Eli Lilly And Company Pvt Ltd

⚠️ High Risk

FEI: 3003764341 • Gurgaon • INDIA

FEI

FEI Number

3003764341

📍

Location

Gurgaon

🇮🇳

Country

INDIA
🏢

Address

Plot 92 Sector 32, , Gurgaon, , India

High Risk

FDA Import Risk Assessment

62.2
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

3
Total Refusals
1
Unique Violations
11/7/2025
Latest Refusal
6/20/2016
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
96.1×20%
Frequency
3.2×10%
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

753×

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

DateProductViolationsDivision
11/7/2025
61PCK74TIRZEPATIDE (ANTI-DIABETIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/31/2025
61PCY74TIRZEPATIDE (ANTI-DIABETIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
6/20/2016
61NCY29FLUOXETINE (ANTI-DEPRESSANT)
75UNAPPROVED
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Eli Lilly And Company Pvt Ltd's FDA import refusal history?

Eli Lilly And Company Pvt Ltd (FEI: 3003764341) has 3 FDA import refusal record(s) in our database, spanning from 6/20/2016 to 11/7/2025.

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. Eli Lilly And Company Pvt Ltd's FEI number is 3003764341.

What types of violations has Eli Lilly And Company Pvt Ltd received?

Eli Lilly And Company Pvt Ltd 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 Eli Lilly And Company Pvt Ltd come from?

All FDA import refusal data for Eli Lilly And Company Pvt Ltd 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.