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SUN PHARMA LAB LTD

⚠️ High Risk

FEI: 3017348001 • Assam • INDIA

FEI

FEI Number

3017348001

📍

Location

Assam

🇮🇳

Country

INDIA
🏢

Address

Pallashbari, , Assam, , India

High Risk

FDA Import Risk Assessment

62.9
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
12/1/2025
Latest Refusal
7/21/2021
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
97.8×20%
Frequency
6.9×10%
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
12/1/2025
66VDB99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/7/2023
62GDK99ANTI-INFLAMMATORY N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/21/2021
66NDY03QUETIAPINE FUMARATE (TRANQUILIZER (ANTI-PSYCHOTIC) - PART II)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SUN PHARMA LAB LTD's FDA import refusal history?

SUN PHARMA LAB LTD (FEI: 3017348001) has 3 FDA import refusal record(s) in our database, spanning from 7/21/2021 to 12/1/2025.

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. SUN PHARMA LAB LTD's FEI number is 3017348001.

What types of violations has SUN PHARMA LAB LTD received?

SUN PHARMA LAB 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 SUN PHARMA LAB LTD come from?

All FDA import refusal data for SUN PHARMA LAB 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.