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SUN PHARMA LABORATORIES LIMITED

⚠️ High Risk

FEI: 3018676062 • Gangtok, Sikkim • INDIA

FEI

FEI Number

3018676062

📍

Location

Gangtok, Sikkim

🇮🇳

Country

INDIA
🏢

Address

107 - 108, , Gangtok, Sikkim, India

High Risk

FDA Import Risk Assessment

65.5
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
12/19/2025
Latest Refusal
12/27/2024
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
98.8×20%
Frequency
30.0×10%
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
12/19/2025
66NCA07OXCARBAZEPINE (TRANQUILIZER (ANTI-PSYCHOTIC) - PART II)
75UNAPPROVED
Division of Southeast Imports (DSEI)
11/20/2025
61MDY99ANTI-CONVULSANT, N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/27/2024
61NCY99ANTI-DEPRESSANT N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is SUN PHARMA LABORATORIES LIMITED's FDA import refusal history?

SUN PHARMA LABORATORIES LIMITED (FEI: 3018676062) has 3 FDA import refusal record(s) in our database, spanning from 12/27/2024 to 12/19/2025.

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 LABORATORIES LIMITED's FEI number is 3018676062.

What types of violations has SUN PHARMA LABORATORIES LIMITED received?

SUN PHARMA LABORATORIES LIMITED 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 LABORATORIES LIMITED come from?

All FDA import refusal data for SUN PHARMA 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.