sun pharma laboratories ltd
⚠️ High Risk
FEI: 3031264870 • Ranipool, Gangtok • INDIA
FEI Number
3031264870
Location
Ranipool, Gangtok
Country
INDIAAddress
plot No 754, Nandok Block, Ranipool, Gangtok, India
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/9/2025 | 61MCC35DIVALPROEX SODIUM (ANTI-CONVULSANT) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 3/31/2025 | 61NCA70LITHIUM (ANTI-DEPRESSANT) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 11/20/2024 | 62TDC07PANTOPRAZOLE SODIUM | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 11/20/2024 | 54AGB13VITAMIN C (ASCORBIC ACID) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 11/20/2024 | 54AGB15VITAMIN D2 (CALCIFEROL) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 8/23/2024 | 60LCA85MESALAMINE (ANALGESIC) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is sun pharma laboratories ltd's FDA import refusal history?
sun pharma laboratories ltd (FEI: 3031264870) has 6 FDA import refusal record(s) in our database, spanning from 8/23/2024 to 12/9/2025.
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 ltd's FEI number is 3031264870.
What types of violations has sun pharma laboratories ltd received?
sun pharma laboratories 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 laboratories ltd come from?
All FDA import refusal data for sun pharma laboratories 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.