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Ipca Laboratories Ltd

⚠️ High Risk

FEI: 3010578430 • Sikkim • INDIA

FEI

FEI Number

3010578430

📍

Location

Sikkim

🇮🇳

Country

INDIA
🏢

Address

393-394 A D Jorethary, Bharihola, Sikkim, , India

High Risk

FDA Import Risk Assessment

65.4
LowModerateHighCritical

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

Statistics

9
Total Refusals
2
Unique Violations
1/2/2026
Latest Refusal
9/12/2016
Earliest Refusal

Score Breakdown

Violation Severity
88.0×40%
Refusal Volume
37.0×30%
Recency
90.7×20%
Frequency
9.7×10%
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

758×

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).

272×

DRUG GMPS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).

Refusal History

DateProductViolationsDivision
1/2/2026
62UCY11DEXTROMETHORPHAN HYDROBROMIDE (ANTI-TUSSIVE/COLD)
75UNAPPROVED
Division of Southeast Imports (DSEI)
6/20/2023
62CCP02ALTHIAZIDE (ANTI-HYPERTENSIVE)
27DRUG GMPS
Division of Southeast Imports (DSEI)
2/7/2023
66VDY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/28/2022
62LCA29HYDROXYCHLOROQUINE SULFATE (ANTI-PROTOZOAL, A-LEISHMANIAL, A-MALARIAL)
75UNAPPROVED
Division of Southeast Imports (DSEI)
3/4/2022
62LCY29HYDROXYCHLOROQUINE SULFATE (ANTI-PROTOZOAL, A-LEISHMANIAL, A-MALARIAL)
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/7/2021
62LCY29HYDROXYCHLOROQUINE SULFATE (ANTI-PROTOZOAL, A-LEISHMANIAL, A-MALARIAL)
27DRUG GMPS
75UNAPPROVED
Division of Northern Border Imports (DNBI)
4/19/2017
62GDA99ANTI-INFLAMMATORY N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
1/4/2017
62LCY29HYDROXYCHLOROQUINE SULFATE (ANTI-PROTOZOAL, A-LEISHMANIAL, A-MALARIAL)
75UNAPPROVED
New Orleans District Office (NOL-DO)
9/12/2016
62OCY09TELMISARTAN (ANTI-HYPERTENSIVE - PART II)
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Ipca Laboratories Ltd's FDA import refusal history?

Ipca Laboratories Ltd (FEI: 3010578430) has 9 FDA import refusal record(s) in our database, spanning from 9/12/2016 to 1/2/2026.

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. Ipca Laboratories Ltd's FEI number is 3010578430.

What types of violations has Ipca Laboratories Ltd received?

Ipca Laboratories Ltd 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 Ipca Laboratories Ltd come from?

All FDA import refusal data for Ipca 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.