Site records / Maharashtra / FEI 3015392060

Lupin LimitedNagpur, Maharashtra

FDA-registered drug establishment in Nagpur, Maharashtra: manufacture, pack. Registration valid to 31 Dec 2026. Record as observed 27 Sep 2026.

Inspections posted
2
Last inspection
Sep 2025 · VAI
Warning letters to this FEI
0
Import alerts at this address
0
US border refusals, 2 years
0
The site dossier

This site, graded.
Every fact sourced.

  • A grade from A to E on a registered ten-factor rubric, with the fact behind every factor
  • Every posted FDA citation, sorted into failure categories and set against Indian drug inspections
  • Warning-letter violations, numbered and labelled
  • Import-alert history rebuilt from the archive, each listing checked against this address
  • Border refusals by product, and the company's other sites, each graded
  • A hash of every source read, so the PDF can be checked against the record

On 2022–26 inspections the rubric never saw, grade E sites were classified OAI 26.5% of the time and grade A sites 4.0%.

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Inspections

2 FDA inspections of this FEI, by end date; 2 with a posted classification.

  1. 16 Sep 2025VAI · Voluntary Action IndicatedDrug Quality Assurance · 6 citations posted
  2. 13 Jun 2024NAI · No Action IndicatedCompliance: Devices, Postmarket Assurance: Devices · no citations posted

Warning letters and compliance actions

  1. 27 Sep 2022Warning letter to Lupin Limited SourceCGMP/Active Pharmaceutical Ingredient (API)/Adulterated · issued to the firm name; FDA does not tie it to this FEI

Import alerts in force

No listing in force under this firm's name.

Form 483s released by FDA

  1. 16 Sep 2025Form 483 · 8 pages Source

Other registered sites of Lupin

Registration

FEI
3015392060
DUNS
675485014
Registered as
LUPIN LIMITED
Registrant
LUPIN LIMITED
Address
Unit-2, Plot No. 6B, Sector - 17, Special Economic Zone, Mihan, Nagpur, Maharashtra 441108, India (IND)
Operations
MANUFACTURE, PACK
Registration expires
31 Dec 2026

Sources: FDA drug establishment registrations, FDA Data Dashboard inspections and compliance actions, import-alert pages, warning letters, import refusals and the FDA reading room, as held in Counterfoil's point-in-time corpus. No matched action does not establish compliance, and FDA registration is not FDA approval. Sources and coverage.

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