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Facility profile

LUPIN LIMITED

Drug product manufacturing · Active pharmaceutical ingredient (API) manufacturing · Madhya Pradesh 462046 · India

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed11 registered company locations
Potential fit

Listed operations

The U.S. Food and Drug Administration (FDA) record lists broad activities for this site. Confirm specific services and availability directly.

Active pharmaceutical ingredient (API) manufactureManufacturePack
Due diligence

Regulatory record at a glance

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Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
Official action indicated (OAI)

Nov 23, 2022 · The findings may warrant official FDA action.

Matched compliance actions
Past action on file · 2019

More than five years old · review later records.

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Shows

Registration status and a latest matched official action indicated inspection.

Doesn’t show

Exact services, availability, capacity, pricing, or overall quality.

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Method and source details
View full inspection and compliance history6 inspection records

FDA inspection history

6 records, Nov 2008 – Nov 2022 · 0 NAI · 3 VAI · 3 OAI

DateClassProject areaCitationsFY
Nov 23, 2022OAIDrug Quality Assurance2023
Dec 4, 2018OAIDrug Quality Assurance2019
Feb 19, 2016VAIDrug Quality Assurance2016
Sep 23, 2011VAIDrug Quality Assurance2011
Nov 30, 2009VAIDrug Quality Assurance2010
Nov 12, 2008OAIDrug Quality Assurance2009

No action indicated (NAI) · Voluntary action indicated (VAI) · Official action indicated (OAI)

Matched compliance actions

Sep 10, 2019Warning Letter · CDER
May 7, 2009Warning Letter · CDER
Unclaimed profile

Service details not yet provided

Methods, equipment, quality scope, capacity, turnaround, and commercial contacts are not available.

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