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HAB PHARMACEUTICALS & RESEARCH

⚠️ High Risk

FEI: 3006076463 • Dehradun • INDIA

FEI

FEI Number

3006076463

📍

Location

Dehradun

🇮🇳

Country

INDIA
🏢

Address

10 Pharmacity, Sidcul, Selaqui, , Dehradun, , India

High Risk

FDA Import Risk Assessment

53.0
LowModerateHighCritical

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

Statistics

4
Total Refusals
3
Unique Violations
8/27/2025
Latest Refusal
2/15/2018
Earliest Refusal

Score Breakdown

Violation Severity
72.9×40%
Refusal Volume
25.9×30%
Recency
78.0×20%
Frequency
5.3×10%
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

754×

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).

1182×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
8/27/2025
66VIY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
Division of Southeast Imports (DSEI)
10/23/2024
62LCY47IVERMECTIN (ANTI-PROTOZOAL, A-LEISHMANIAL, ANTI-MALARIAL)
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Division of Southeast Imports (DSEI)
12/15/2020
65PCA02SILDENAFIL CITRATE (REGULATOR)
118NOT LISTED
75UNAPPROVED
Division of Northern Border Imports (DNBI)
2/15/2018
61ECA09MONTELUKAST SODIUM (ANTI-ASTHMATIC)
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is HAB PHARMACEUTICALS & RESEARCH's FDA import refusal history?

HAB PHARMACEUTICALS & RESEARCH (FEI: 3006076463) has 4 FDA import refusal record(s) in our database, spanning from 2/15/2018 to 8/27/2025.

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. HAB PHARMACEUTICALS & RESEARCH's FEI number is 3006076463.

What types of violations has HAB PHARMACEUTICALS & RESEARCH received?

HAB PHARMACEUTICALS & RESEARCH has been cited for 3 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 HAB PHARMACEUTICALS & RESEARCH come from?

All FDA import refusal data for HAB PHARMACEUTICALS & RESEARCH 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.