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Intas Pharmaceuticals Limited

FDA import alert and refusal historyAhmedabad, IndiaFEI 3003157498

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Example subjectIntas Pharmaceuticals Limite added to Import Alert 16-129 (red list)

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As of October 26, 2026, Intas Pharmaceuticals Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on January 18, 2026, most often for drug gmps (DRUG GMPS).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · DRUG GMPS
Last warning letter
None found
Last inspection
None on record

Every FDA record for Intas Pharmaceuticals Limited

1 record, newest first. Each line links to the FDA page it came from.

2026

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.DRUG GMPSEntry AEK-9092558-5
    Source

Refusal charges, in plain English

Questions about Intas Pharmaceuticals Limited

Is Intas Pharmaceuticals Limited on an FDA import alert?
No listing for Intas Pharmaceuticals Limited appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the India page.
Has FDA refused shipments from Intas Pharmaceuticals Limited?
Yes. FDA refused 1 shipment line from Intas Pharmaceuticals Limited on January 18, 2026. The most recent, on January 18, 2026, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as DRUG GMPS (drug gmps).
Why did FDA refuse Intas Pharmaceuticals Limited's shipments?
The most frequent charge is DRUG GMPS (drug gmps, 1 line).
What is Intas Pharmaceuticals Limited's FEI number?
Intas Pharmaceuticals Limited's FDA Establishment Identifier (FEI) is 3003157498.

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Example subjectIntas Pharmaceuticals Limite added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.