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Ipca Laboratories

⚠️ High Risk

FEI: 3006415843 • Dehradun • INDIA

FEI

FEI Number

3006415843

📍

Location

Dehradun

🇮🇳

Country

INDIA
🏢

Address

C-6 Sara Ind. Estate, Chakrata Road, Rampur, Dehradun, , India

High Risk

FDA Import Risk Assessment

58.3
LowModerateHighCritical

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

Statistics

6
Total Refusals
1
Unique Violations
8/9/2024
Latest Refusal
5/22/2020
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
31.3×30%
Recency
57.2×20%
Frequency
14.2×10%
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

756×

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
8/9/2024
60LDA01ACETAMINOPHEN (ANALGESIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/12/2023
62GCB99ANTI-INFLAMMATORY N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/30/2021
62LCA36QUININE DIHYDROCHLORIDE (ANTI-PROTOZOAL, A-LEISHMANIAL, A-MALARIAL)
75UNAPPROVED
Division of Southeast Imports (DSEI)
4/3/2021
65CDB99NUTRIENT/TONIC N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
9/30/2020
61PDA99ANTI-DIABETIC N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
5/22/2020
62LCA29HYDROXYCHLOROQUINE SULFATE (ANTI-PROTOZOAL, A-LEISHMANIAL, A-MALARIAL)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Ipca Laboratories's FDA import refusal history?

Ipca Laboratories (FEI: 3006415843) has 6 FDA import refusal record(s) in our database, spanning from 5/22/2020 to 8/9/2024.

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's FEI number is 3006415843.

What types of violations has Ipca Laboratories received?

Ipca Laboratories 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 Ipca Laboratories come from?

All FDA import refusal data for Ipca Laboratories 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.