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    Company profile for Sun Pharmaceutical Industries Limited

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    EVENTS

    DIGITAL CONTENT

    ACTIVE PHARMA INGREDIENTS

    DEVELOPMENTS

    FINISHED DOSAGE FORMULATIONS

    EXCIPIENTS

    REF. STANDARDS & IMPURITIES

    INSPECTIONS & REGISTRATIONS

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    About

    We were pioneers among Indian pharmaceutical companies to see tremendous value in investing in research & development (R&D). Our early investments in R&D, beginning three decades ago, enabled us to make technology our key differentiator and develop a basket of robust products for diverse markets across the world. Our core strength lies in our ability to excel in developing generics and technologically complex products through ...
    We were pioneers among Indian pharmaceutical companies to see tremendous value in investing in research & development (R&D). Our early investments in R&D, beginning three decades ago, enabled us to make technology our key differentiator and develop a basket of robust products for diverse markets across the world. Our core strength lies in our ability to excel in developing generics and technologically complex products through focused teams in formulations, process chemistry and analytical development. We have the capability to deliver quality products within established timelines, at low costs and without compromising on quality.

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    CONTACT DETAILS

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    Sun Pharmaceutical Industries Limitedindia-flag Flag
    Country
    Country
    India
    Address
    Address
    Sun House, CTS No. 201 B/1, Western Express Highway, Goregaon (E), Mumbai 400...
    Telephone
    Telephone
    Client Email
    Email
    enquiries@pharmacompass.com
    Client Website
    Website
    https://sunpharma.com/
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    Linkedin
    https://in.linkedin.com/company/sun-pharma
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    Twitter
    https://x.com/SunPharma_Live?ref

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    Events

    Webinars & Exhibitions

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    NEWS #PharmaBuzz

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    Sun Pharma Gets Relief In Trademark Case From High Court
    Sun Pharma Gets Relief In Trademark Case From High Court

    07 May 2026

    // ECONOMICTIMES

    https://economictimes.indiatimes.com/industry/healthcare/biotech/pharmaceuticals/sun-pharma-gets-relief-in-trademark-case-from-high-court/articleshow/130867916.cms

    ECONOMICTIMES
    07 May 2026
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    Sun Pharma Explores Funding Mix For $12 Billion Organon Deal
    Sun Pharma Explores Funding Mix For $12 Billion Organon Deal

    06 May 2026

    // ECONOMICTIMES

    https://economictimes.indiatimes.com/industry/healthcare/biotech/pharmaceuticals/sun-pharma-explores-funding-mix-for-12-billion-organon-deal/articleshow/130841915.cms

    ECONOMICTIMES
    06 May 2026
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    Sun Pharma Canada’s Generics Doxepin HCl Receives Approval in US
    Sun Pharma Canada’s Generics Doxepin HCl Receives Approval in US

    28 Apr 2026

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=213919

    FDA
    28 Apr 2026
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    Sun Pharma signs Definitive Agreement to Acquire Organon
    Sun Pharma signs Definitive Agreement to Acquire Organon

    27 Apr 2026

    // BUSINESSWIRE

    https://www.businesswire.com/news/home/20260426881370/en/Sun-Pharma-signs-Definitive-Agreement-to-Acquire-Organon

    BUSINESSWIRE
    27 Apr 2026
    Share Share
    Halper Sadeh Probes Organon & Co. Shareholder Deal Equity
    Halper Sadeh Probes Organon & Co. Shareholder Deal Equity

    27 Apr 2026

    // PHARMIWEB

    https://www.pharmiweb.com/press-release/2026-04-27/ogn-stock-alert-halper-sadeh-llc-is-investigating-whether-organon-co-is-obtaining-a-fair-price-f

    PHARMIWEB
    27 Apr 2026
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    Sun Pharma Wins Trademark Case Against Navi Mumbai Company
    Sun Pharma Wins Trademark Case Against Navi Mumbai Company

    24 Apr 2026

    // ECONOMICTIMES

    https://economictimes.indiatimes.com/industry/healthcare/biotech/pharmaceuticals/sun-pharma-wins-trademark-case-against-navi-mumbai-company/articleshow/130477715.cms

    ECONOMICTIMES
    24 Apr 2026
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    USDMF

    read-more
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    01

    Abiraterone Acetate

    India
    RDD
    Not Confirmed
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    02

    Acitretin Usp

    India
    RDD
    Not Confirmed
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    03

    Acitretin Usp

    India
    RDD
    Not Confirmed
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    04

    Acyclovir Drug Substance

    India
    RDD
    Not Confirmed
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    05

    Adefovir Dipivoxil

    India
    RDD
    Not Confirmed
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    06

    Afatinib Dimaleate

    India
    RDD
    Not Confirmed
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    07

    Alectinib Hydrochloride

    India
    RDD
    Not Confirmed
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    08

    Alendronate Sodium Usp

    India
    RDD
    Not Confirmed
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    09

    Aluminum Chlorhydroxide Complex Ach-...

    U.S.A
    RDD
    Not Confirmed
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    10

    Ambrisentan

    India
    RDD
    Not Confirmed
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    CEP/COS

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    01

    Aciclovir

    CEP/COS

    RDD
    Not Confirmed
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    02

    Amisulpride

    CEP/COS

    RDD
    Not Confirmed
    arrow

    03

    Amisulpride, Process II

    CEP/COS

    RDD
    Not Confirmed
    arrow

    04

    Amoxicillin trihydrate

    CEP/COS

    RDD
    Not Confirmed
    arrow

    05

    Atorvastatin calcium, Process-VIII

    CEP/COS

    RDD
    Not Confirmed
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    06

    Benazepril hydrochloride

    CEP/COS

    RDD
    Not Confirmed
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    07

    Budesonide

    CEP/COS

    RDD
    Not Confirmed
    arrow

    08

    Buprenorphine hydrochloride

    CEP/COS

    RDD
    Not Confirmed
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    09

    Candesartan cilexetil

    CEP/COS

    RDD
    Not Confirmed
    arrow

    10

    Candesartan cilexetil, Process-IV

    CEP/COS

    RDD
    Not Confirmed
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    JDMF

    read-more
    read-more

    01

    Bicalutamide

    JDMF

    RDD
    Not Confirmed
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    Bicalutamide

    India
    arrow
    RDD
    Not Confirmed
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    Sun Pharmaceutical Industries Limited

    Registration Number : 226MF10195

    Registrant's Address : SUN HOUSE, Plot No. 201 B/1, Western Express Highway, Goregaon (E), Mumbai 400063, Ma...

    Initial Date of Registration : 2014-10-27

    Latest Date of Registration : 2014-10-27

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    02

    CEFPODOXIME PROXETIL

    JDMF

    RDD
    Not Confirmed
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    CEFPODOXIME PROXETIL

    India
    arrow
    RDD
    Not Confirmed
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    Sun Pharmaceutical Industries Limited

    Registration Number : 222MF10026

    Registrant's Address : Plot No. 90, Sector 32, Gurgaon, Haryana 122011, India

    Initial Date of Registration : 2010-01-22

    Latest Date of Registration : 2010-01-22

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    03

    Cilazapril

    JDMF

    RDD
    Not Confirmed
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    Cilazapril

    India
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    RDD
    Not Confirmed
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    Sun Pharmaceutical Industries Limited

    Registration Number : 219MF10214

    Registrant's Address : SUN HOUSE, Plot No. 201 B/1, Western Express Highway, Goregaon (E), Mumbai 400063, Ma...

    Initial Date of Registration : 2007-06-25

    Latest Date of Registration : 2007-06-25

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    04

    Clarithromycin

    JDMF

    RDD
    Not Confirmed
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    Clarithromycin

    India
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    RDD
    Not Confirmed
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    Sun Pharmaceutical Industries Limited

    Registration Number : 220MF10255

    Registrant's Address : Plot No. 90, Sector 32, Gurgaon, Haryana 122 001, India　

    Initial Date of Registration : 2008-12-12

    Latest Date of Registration : 2008-12-12

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    05

    FLUVOXAMINE MALEATE

    JDMF

    RDD
    Not Confirmed
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    FLUVOXAMINE MALEATE

    India
    arrow
    RDD
    Not Confirmed
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    Sun Pharmaceutical Industries Limited

    Registration Number : 221MF10042

    Registrant's Address : SUN HOUSE, Plot No. 201 B/1, Western Express Highway, Goregaon (E), Mumbai 400063, Ma...

    Initial Date of Registration : 2009-02-23

    Latest Date of Registration : 2009-02-23

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    06

    GEMCITABINE HYDROCHLORIDE

    JDMF

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    Not Confirmed
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    GEMCITABINE HYDROCHLORIDE

    India
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    RDD
    Not Confirmed
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    Sun Pharmaceutical Industries Limited

    Registration Number : 221MF10018

    Registrant's Address : SUN HOUSE, Plot No. 201 B/1, Western Express Highway, Goregaon (E), Mumbai 400063, Ma...

    Initial Date of Registration : 2009-01-28

    Latest Date of Registration : 2009-01-28

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    07

    Levofloxacin

    JDMF

    RDD
    Not Confirmed
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    Levofloxacin

    India
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    RDD
    Not Confirmed
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    Sun Pharmaceutical Industries Limited

    Registration Number : 218MF10720

    Registrant's Address : Plot No. 90, Sector 32 Gurgaon Haryana -122011 India

    Initial Date of Registration : 2006-09-06

    Latest Date of Registration : 2006-09-06

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    08

    Luliconazole

    JDMF

    RDD
    Not Confirmed
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    Luliconazole

    India
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    RDD
    Not Confirmed
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    Sun Pharmaceutical Industries Limited

    Registration Number : 301MF10097

    Registrant's Address : SUN HOUSE, Plot No. 201 B/1, Western Express Highway, Goregaon (E), Mumbai 400063, Ma...

    Initial Date of Registration : 2019-11-19

    Latest Date of Registration : 2019-11-19

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    09

    Meropenem hydrate

    JDMF

    RDD
    Not Confirmed
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    Meropenem hydrate

    India
    arrow
    RDD
    Not Confirmed
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    Sun Pharmaceutical Industries Limited

    Registration Number : 220MF10004

    Registrant's Address : SUN HOUSE, Plot No. 201 B/1, Western Express Highway, Goregaon (E), Mumbai 400063, Ma...

    Initial Date of Registration : 2008-01-09

    Latest Date of Registration : 2008-01-09

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    10

    Mesalazine (production only)

    JDMF

    RDD
    Not Confirmed
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    Mesalazine (production only)

    India
    arrow
    RDD
    Not Confirmed
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    Sun Pharmaceutical Industries Limited

    Registration Number : 219MF10100

    Registrant's Address : SUN HOUSE, Plot No. 201 B/1, Western Express Highway, Goregaon (E), Mumbai 400063, Ma...

    Initial Date of Registration : 2007-03-14

    Latest Date of Registration : 2007-03-14

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    EU WC

    read-more
    read-more

    01

    Abiraterone Acetate IH

    India
    RDD
    Not Confirmed
    arrow

    02

    Acitretin USP

    India
    RDD
    Not Confirmed
    arrow

    03

    Sodium Alendronate BP/Ph.Eur...

    India
    RDD
    Not Confirmed
    arrow

    04

    Alendronate Sodium USP

    India
    RDD
    Not Confirmed
    arrow

    05

    Amifostine USP

    India
    RDD
    Not Confirmed
    arrow

    06

    Amisulpride BP/EP

    India
    RDD
    Not Confirmed
    arrow

    07

    Amitriptyline Hydrochloride ...

    India
    RDD
    Not Confirmed
    arrow

    08

    Amorolfine Hydrochloride Ph....

    India
    RDD
    Not Confirmed
    arrow

    09

    Anastrozole USP/EP

    India
    RDD
    Not Confirmed
    arrow

    10

    Atomoxetin Hydrochloride USP...

    India
    RDD
    Not Confirmed
    arrow
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    NDC API

    read-more
    read-more

    01

    ABIRATERONE ACETATE

    India
    RDD
    Not Confirmed
    arrow

    02

    ACITRETIN

    India
    RDD
    Not Confirmed
    arrow

    ACITRETIN

    India
    arrow
    RDD
    Not Confirmed
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    Sun Pharmaceutical Industries Limited

    NDC Package Code : 62756-269

    Start Marketing Date : 2021-01-15

    End Marketing Date : 2026-12-31

    Dosage Form (Strength) : POWDER (5kg/5kg)

    Marketing Category : BULK INGREDIENT

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    03

    AFATINIB DIMALEATE

    India
    RDD
    Not Confirmed
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    04

    ALECTINIB HYDROCHLORIDE

    India
    RDD
    Not Confirmed
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    05

    ALENDRONATE SODIUM

    India
    RDD
    Not Confirmed
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    06

    AMIFOSTINE

    India
    RDD
    Not Confirmed
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    07

    ANASTROZOLE

    India
    RDD
    Not Confirmed
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    08

    APREMILAST

    India
    RDD
    Not Confirmed
    arrow

    APREMILAST

    India
    arrow
    RDD
    Not Confirmed
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    Sun Pharmaceutical Industries Limited

    NDC Package Code : 62756-690

    Start Marketing Date : 2018-06-26

    End Marketing Date : 2027-12-31

    Dosage Form (Strength) : POWDER (25kg/25kg)

    Marketing Category : BULK INGREDIENT

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    09

    ARIPIPRAZOLE

    India
    RDD
    Not Confirmed
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    ARIPIPRAZOLE

    India
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    RDD
    Not Confirmed
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    Sun Pharmaceutical Industries Limited

    NDC Package Code : 62756-919

    Start Marketing Date : 2025-03-11

    End Marketing Date : 2026-12-31

    Dosage Form (Strength) : POWDER (25kg/25kg)

    Marketing Category : BULK INGREDIENT

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    10

    ASENAPINE MALEATE

    India
    RDD
    Not Confirmed
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    FDA Orange Book

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    01

    Brand Name : YONSA

    India
    RDD
    Not Confirmed
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    Brand Name : YONSA

    India
    RDD
    Not Confirmed
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    RLD : Yes

    TE Code :

    ABIRATERONE ACETATE

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET; ORAL

    Proprietary Name : YONSA

    Dosage Strength : 125MG

    Approval Date : 2018-05-22

    Application Number : 210308

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    02

    Brand Name : ACETAMINOPHEN

    India
    RDD
    Not Confirmed
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    Brand Name : ACETAMINOPHEN

    India
    RDD
    Not Confirmed
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    RLD : No

    TE Code :

    ACETAMINOPHEN

    Sun Pharmaceutical Industries Limited

    Dosage Form : SUPPOSITORY; RECTAL

    Proprietary Name : ACETAMINOPHEN

    Dosage Strength : 120MG

    Approval Date : 1995-02-27

    Application Number : 73106

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    Brand Name : ACETAMINOPHEN

    India
    RDD
    Not Confirmed
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    Brand Name : ACETAMINOPHEN

    India
    RDD
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    RLD : No

    TE Code :

    ACETAMINOPHEN

    Sun Pharmaceutical Industries Limited

    Dosage Form : SUPPOSITORY; RECTAL

    Proprietary Name : ACETAMINOPHEN

    Dosage Strength : 325MG

    Approval Date : 1995-02-27

    Application Number : 73107

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    Brand Name : ACETAMINOPHEN

    India
    RDD
    Not Confirmed
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    Brand Name : ACETAMINOPHEN

    India
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    RLD : No

    TE Code :

    ACETAMINOPHEN

    Sun Pharmaceutical Industries Limited

    Dosage Form : SUPPOSITORY; RECTAL

    Proprietary Name : ACETAMINOPHEN

    Dosage Strength : 650MG

    Approval Date : 1995-02-27

    Application Number : 73108

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    Brand Name : ACETAMINOPHEN

    India
    RDD
    Not Confirmed
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    Brand Name : ACETAMINOPHEN

    India
    RDD
    Not Confirmed
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    RLD : No

    TE Code :

    ACETAMINOPHEN

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : ACETAMINOPHEN

    Dosage Strength : 650MG

    Approval Date : 2002-03-19

    Application Number : 76200

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    06

    Brand Name : ACETAMINOPHEN

    India
    RDD
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    Brand Name : ACETAMINOPHEN

    India
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    RLD : No

    TE Code :

    ACETAMINOPHEN

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : ACETAMINOPHEN

    Dosage Strength : 650MG

    Approval Date : 2011-12-14

    Application Number : 78569

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    Brand Name : ACETAMINOPHEN

    India
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    Brand Name : ACETAMINOPHEN

    India
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    RLD : No

    TE Code :

    ACETAMINOPHEN

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : ACETAMINOPHEN

    Dosage Strength : 650MG

    Approval Date : 2009-11-18

    Application Number : 90205

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    Brand Name : BUTALBITAL, ACETAMIN...

    India
    RDD
    Not Confirmed
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    Brand Name : BUTALBITAL, ACETAMIN...

    India
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    RLD : No

    TE Code :

    ACETAMINOPHEN; BUTALBITAL; CAFFEINE

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET; ORAL

    Proprietary Name : BUTALBITAL, ACETAMINOPHE...

    Dosage Strength : 325MG;50MG;40MG

    Approval Date : 2001-07-23

    Application Number : 40390

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    09

    Brand Name : BUTALBITAL, ACETAMIN...

    India
    RDD
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    Brand Name : BUTALBITAL, ACETAMIN...

    India
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    RLD : No

    TE Code :

    ACETAMINOPHEN; BUTALBITAL; CAFFEINE

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET; ORAL

    Proprietary Name : BUTALBITAL, ACETAMINOPHE...

    Dosage Strength : 500MG;50MG;40MG

    Approval Date : 2001-07-23

    Application Number : 40394

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    Brand Name : BUTALBITAL, ACETAMIN...

    India
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    RLD : No

    TE Code :

    ACETAMINOPHEN; BUTALBITAL; CAFFEINE

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET; ORAL

    Proprietary Name : BUTALBITAL, ACETAMINOPHE...

    Dosage Strength : 325MG;50MG;40MG

    Approval Date : 2005-07-29

    Application Number : 40601

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    Canada

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    01

    Brand Name : TARO-TRAMADOL/ACET

    India
    RDD
    Not Confirmed
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    Brand Name : TARO-TRAMADOL/ACET

    India
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    Regulatory Info : NARCOTICS (CDSA I)

    Registration Country : Canada

    ACETAMINOPHEN

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET

    Dosage Strength : 325MG

    Packaging : 100

    Brand Name : TARO-TRAMADOL/ACET

    Approval Date :

    Application Number : 2388197

    Regulatory Info : NARCOTICS (CDSA I)

    Registration Country : Canada

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    02

    Brand Name : LEVULAN KERASTICK

    India
    RDD
    Not Confirmed
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    Brand Name : LEVULAN KERASTICK

    India
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    RDD
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    Regulatory Info : PRESCRIPTION

    Registration Country : Canada

    AMINOLEVULINIC ACID HYDROCHLORIDE

    Sun Pharmaceutical Industries Limited

    Dosage Form : POWDER FOR SOLUTION

    Dosage Strength : 20%/W/V

    Packaging :

    Brand Name : LEVULAN KERASTICK

    Approval Date :

    Application Number : 2243933

    Regulatory Info : PRESCRIPTION

    Registration Country : Canada

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    03

    Brand Name : TARO-APIXABAN

    India
    RDD
    Not Confirmed
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    Brand Name : TARO-APIXABAN

    India
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    RDD
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    Regulatory Info : PRESCRIPTION

    Registration Country : Canada

    APIXABAN

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET

    Dosage Strength : 2.5MG

    Packaging :

    Brand Name : TARO-APIXABAN

    Approval Date :

    Application Number : 2510464

    Regulatory Info : PRESCRIPTION

    Registration Country : Canada

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    Brand Name : TARO-APIXABAN

    India
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    Brand Name : TARO-APIXABAN

    India
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    Regulatory Info : PRESCRIPTION

    Registration Country : Canada

    APIXABAN

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET

    Dosage Strength : 5MG

    Packaging :

    Brand Name : TARO-APIXABAN

    Approval Date :

    Application Number : 2510472

    Regulatory Info : PRESCRIPTION

    Registration Country : Canada

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    05

    Brand Name : TARO-ATENOLOL

    India
    RDD
    Not Confirmed
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    Brand Name : TARO-ATENOLOL

    India
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    Regulatory Info : PRESCRIPTION

    Registration Country : Canada

    ATENOLOL

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET

    Dosage Strength : 50MG

    Packaging : 30/100/500

    Brand Name : TARO-ATENOLOL

    Approval Date :

    Application Number : 2267985

    Regulatory Info : PRESCRIPTION

    Registration Country : Canada

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    Brand Name : TARO-ATENOLOL

    India
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    Brand Name : TARO-ATENOLOL

    India
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    Regulatory Info : PRESCRIPTION

    Registration Country : Canada

    ATENOLOL

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET

    Dosage Strength : 100MG

    Packaging : 30/100/500

    Brand Name : TARO-ATENOLOL

    Approval Date :

    Application Number : 2267993

    Regulatory Info : PRESCRIPTION

    Registration Country : Canada

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    07

    Brand Name : TARO-ATENOLOL

    India
    RDD
    Not Confirmed
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    Brand Name : TARO-ATENOLOL

    India
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    RDD
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    Regulatory Info : PRESCRIPTION

    Registration Country : Canada

    ATENOLOL

    Sun Pharmaceutical Industries Limited

    Dosage Form : TABLET

    Dosage Strength : 25MG

    Packaging : 100

    Brand Name : TARO-ATENOLOL

    Approval Date :

    Application Number : 2373963

    Regulatory Info : PRESCRIPTION

    Registration Country : Canada

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    08

    Brand Name : PROACTIV+ SKIN SMOOT...

    U.S.A
    RDD
    Not Confirmed
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    Brand Name : PROACTIV+ SKIN SMOOT...

    U.S.A
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    Not Confirmed
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    Regulatory Info : NON-PRESCRIPTION DRUGS

    Registration Country : Canada

    BENZOYL PEROXIDE

    Alchemee

    Dosage Form : GEL

    Dosage Strength : 2.5%/W/W

    Packaging : 60ML/177.4ML

    Brand Name : PROACTIV+ SKIN SMOOTHING EXFO...

    Approval Date :

    Application Number : 2394421

    Regulatory Info : NON-PRESCRIPTION DRUGS

    Registration Country : Canada

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    Brand Name : PROACTIV EMERGENCY B...

    U.S.A
    RDD
    Not Confirmed
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    Brand Name : PROACTIV EMERGENCY B...

    U.S.A
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    RDD
    Not Confirmed
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    Regulatory Info : NON-PRESCRIPTION DRUGS

    Registration Country : Canada

    BENZOYL PEROXIDE

    Alchemee

    Dosage Form : CREAM

    Dosage Strength : 5%/W/W

    Packaging : 177.4ML-6 FL OZ

    Brand Name : PROACTIV EMERGENCY BLEMISH RE...

    Approval Date :

    Application Number : 2413655

    Regulatory Info : NON-PRESCRIPTION DRUGS

    Registration Country : Canada

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    Brand Name : PROACTIV+ 3 PIECE SE...

    U.S.A
    RDD
    Not Confirmed
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    Brand Name : PROACTIV+ 3 PIECE SE...

    U.S.A
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    RDD
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    Regulatory Info : NON-PRESCRIPTION DRUGS

    Registration Country : Canada

    BENZOYL PEROXIDE

    Alchemee

    Dosage Form : GEL

    Dosage Strength : 2.5%/W/W

    Packaging : EXFOLIATOR:60/90/1...

    Brand Name : PROACTIV+ 3 PIECE SET

    Approval Date :

    Application Number : 2414422

    Regulatory Info : NON-PRESCRIPTION DRUGS

    Registration Country : Canada

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    Excipients

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    01

    POLY (LACTIC-CO-GLYCOLIC ACID) (PLG...

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    RDD
    Not Confirmed
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    POLY (LACTIC-CO-GLYCOLIC ACID) (PLG...

    India

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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    USDMF arrow-down Click Us! arrow-down
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 39685

    Submission : 2024-03-29

    Status : Active

    Type : IV

     CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
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    [DL]-POLYLACTIC ACID OR [DL]-PLA-2

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    RDD
    Not Confirmed
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    [DL]-POLYLACTIC ACID OR [DL]-PLA-2

    India

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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    RDD
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    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 40876

    Submission : 2025-03-26

    Status : Active

    Type : IV

     CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
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    Hypromellose Phthalate

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

    RDD
    Not Confirmed
    arrow

    Hypromellose Phthalate

    India

    USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others

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    RDD
    Not Confirmed
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    USDMF Inactive-api
    ✖

    GDUFA

    DMF Review : N/A

    Rev. Date :

    Pay. Date :

    DMF Number : 17589

    Submission : 2004-08-06

    Status : Inactive

    Type : IV

     CEP/COS JDMF EU-WC NDC KDMF VMF Others AUDIT
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    REF. STANDARDS & IMPURITIES

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    Inspections and registrations

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    FDA

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    01

    FDA Audited

    USA
    RDD
    Not Confirmed
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    FDA Audited

    USA
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    RDD
    Not Confirmed

    District Decision : No Action Indicated

    Inspection End Date : 2025-07-18

    Sun Pharmaceutical Industries Limited

    City : Kanchipuram

    State :

    Country/Area : India

    Zip :

    District :

    Center :

    Project Area : Drug Quality Assurance

    District Decision : No Action Indicated

    Inspection End Date : 2025-07-18

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    FDA Audited

    USA
    RDD
    Not Confirmed
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    FDA Audited

    USA
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    RDD
    Not Confirmed

    District Decision : Official Action Indicated

    Inspection End Date : 2025-06-13

    Sun Pharmaceutical Industries Limited

    City : Halol

    State :

    Country/Area : India

    Zip :

    District :

    Center :

    Project Area : Drug Quality Assurance

    District Decision : Official Action Indicated

    Inspection End Date : 2025-06-13

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    03

    FDA Audited

    USA
    RDD
    Not Confirmed
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    FDA Audited

    USA
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    RDD
    Not Confirmed

    District Decision : No Action Indicated

    Inspection End Date : 2025-06-13

    Sun Pharmaceutical Industries Limited

    City : Panoli

    State :

    Country/Area : India

    Zip :

    District :

    Center :

    Project Area : Drug Quality Assurance

    District Decision : No Action Indicated

    Inspection End Date : 2025-06-13

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    04

    FDA Audited

    USA
    RDD
    Not Confirmed
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    FDA Audited

    USA
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    RDD
    Not Confirmed

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2025-04-18

    Sun Pharmaceutical Industries Limited

    City : Billerica

    State : Massachusetts

    Country/Area : U.S.A

    Zip : 1821

    District :

    Center :

    Project Area : Drug Quality Assurance

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2025-04-18

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    05

    FDA Audited

    USA
    RDD
    Not Confirmed
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    FDA Audited

    USA
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    RDD
    Not Confirmed

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2025-03-12

    Alkaloida Chemical Company Zrt

    City : Tiszavasvari

    State :

    Country/Area : Hungary

    Zip :

    District :

    Center :

    Project Area : Drug Quality Assurance

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2025-03-12

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    06

    FDA Audited

    USA
    RDD
    Not Confirmed
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    FDA Audited

    USA
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    RDD
    Not Confirmed

    District Decision : No Action Indicated

    Inspection End Date : 2024-12-12

    Sun Pharmaceutical Industries Limited

    City : Princeton

    State : New Jersey

    Country/Area : U.S.A

    Zip : 8540

    District :

    Center :

    Project Area : Bioresearch Monitoring

    District Decision : No Action Indicated

    Inspection End Date : 2024-12-12

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    07

    FDA Audited

    USA
    RDD
    Not Confirmed
    arrow

    FDA Audited

    USA
    arrow
    RDD
    Not Confirmed

    District Decision : No Action Indicated

    Inspection End Date : 2024-10-31

    RANBAXY LABORATORIES LIMITED

    City : New Brunswick

    State : New Jersey

    Country/Area : U.S.A

    Zip : 8901

    District :

    Center :

    Project Area : Drug Quality Assurance

    District Decision : No Action Indicated

    Inspection End Date : 2024-10-31

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    08

    FDA Audited

    USA
    RDD
    Not Confirmed
    arrow

    FDA Audited

    USA
    arrow
    RDD
    Not Confirmed

    District Decision : No Action Indicated

    Inspection End Date : 2024-09-20

    Sun Pharmaceutical Industries Limited

    City : Brampton

    State :

    Country/Area : Canada

    Zip :

    District :

    Center :

    Project Area : Bioresearch Monitoring

    District Decision : No Action Indicated

    Inspection End Date : 2024-09-20

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    09

    FDA Audited

    USA
    RDD
    Not Confirmed
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    FDA Audited

    USA
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    RDD
    Not Confirmed

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2024-05-17

    Sun Pharmaceutical Industries Limited

    City : Bharuch

    State :

    Country/Area : India

    Zip :

    District :

    Center :

    Project Area : Drug Quality Assurance

    District Decision : Voluntary Action Indicated

    Inspection End Date : 2024-05-17

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    10

    FDA Audited

    USA
    RDD
    Not Confirmed
    arrow

    FDA Audited

    USA
    arrow
    RDD
    Not Confirmed

    District Decision : No Action Indicated

    Inspection End Date : 2024-02-15

    Sun Pharmaceutical Industries Limited

    City : Lexington

    State : Massachusetts

    Country/Area : U.S.A

    Zip : 2421

    District :

    Center :

    Project Area : Bioresearch Monitoring

    District Decision : No Action Indicated

    Inspection End Date : 2024-02-15

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    EDQM

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    01

    GMP Certified

    EU
    RDD
    Not Confirmed
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    GMP Certified

    EU
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    RDD
    Not Confirmed

    Sun Pharmaceutical Industries Limited

    Type : GMP Certificates

    Number : GIF-IW-N-40...

    EudraGMDP Key : 9347

    Country : U.S.A

    Issue Date : 2013-08-20

    Post Code : NJ 08901

    NCA Ref : WTN494

    City : New Brunswick

    blank

    Product
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    Stock Recap
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    02

    GMP Certified

    EU
    RDD
    Not Confirmed
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    GMP Certified

    EU
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    RDD
    Not Confirmed

    Sun Pharmaceutical Industries Limited

    Type : GMP Certificates

    Number : UK GMP 2010...

    EudraGMDP Key : 7214

    Country : India

    Issue Date :

    Post Code : 389 350

    NCA Ref : 116444-SUN P...

    City : HALOL

    blank

    Product
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    03

    GMP Certified

    EU
    RDD
    Not Confirmed
    arrow

    GMP Certified

    EU
    arrow
    RDD
    Not Confirmed

    Sun Pharmaceutical Industries Limited

    Type : GMP Certificates

    Number : GIF-IW-N-40...

    EudraGMDP Key : 9347

    Country : India

    Issue Date :

    Post Code : NJ 08901

    NCA Ref : WTN494

    City : New Brunswick

    blank

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Data Compilation
    #PharmaFlow

    04

    GMP Certified

    EU
    RDD
    Not Confirmed
    arrow

    GMP Certified

    EU
    arrow
    RDD
    Not Confirmed

    Sun Pharmaceutical Industries Limited

    Type : GMP Certificates

    Number : NL/H 10/011...

    EudraGMDP Key : 10150

    Country : India

    Issue Date :

    Post Code : 389350

    NCA Ref : 1.015012931e...

    City : Halol

    blank

    Product
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    Stock Recap
    #PipelineProspector

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    05

    GMP Certified

    EU
    RDD
    Not Confirmed
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    GMP Certified

    EU
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    RDD
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    Sun Pharmaceutical Industries Limited

    Type : GMP Certificates

    Number : NL/H 09/007...

    EudraGMDP Key : 9361

    Country : India

    Issue Date :

    Post Code : 414 111

    NCA Ref : 9.3611283284...

    City : Ahmednagar

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    06

    GMP Certified

    EU
    RDD
    Not Confirmed
    arrow

    GMP Certified

    EU
    arrow
    RDD
    Not Confirmed

    Sun Pharmaceutical Industries Limited

    Type : GMP Certificates

    Number : GIF-IW-N-40...

    EudraGMDP Key : 9347

    Country : India

    Issue Date :

    Post Code : NJ 08901

    NCA Ref : WTN494

    City : New Brunswick

    blank

    Product
    Web Link

    Stock Recap
    #PipelineProspector

    Data Compilation
    #PharmaFlow

    07

    GMP Certified

    EU
    RDD
    Not Confirmed
    arrow

    08

    GMP Certified

    EU
    RDD
    Not Confirmed
    arrow

    GMP Certified

    EU
    arrow
    RDD
    Not Confirmed

    Sun Pharmaceutical Industries Limited

    Type : GMP Certificates

    Number : 031/2010/RO

    EudraGMDP Key : 9273

    Country : India

    Issue Date :

    Post Code : 173025

    NCA Ref : 9.2731280143...

    City : Paonta Sahib

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    09

    GMP Certified

    EU
    RDD
    Not Confirmed
    arrow

    10

    GMP Certified

    EU
    RDD
    Not Confirmed
    arrow

    GMP Certified

    EU
    arrow
    RDD
    Not Confirmed

    Sun Pharmaceutical Industries Limited

    Type : GMP Certificates

    Number : 2007/HMP/PT...

    EudraGMDP Key : 8736

    Country : India

    Issue Date :

    Post Code : 173 025

    NCA Ref : A055 9366 60...

    City : PAHONTA SANBIB

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    Only 10 entries up to this point, click to access all click full view read-more
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    Full Screen ViewFULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]

    THIRD-PARTY AUDIT

    read-more
    read-more

    01

    Eurofins Assurance

    Belgium
    arrow
    Get Site Audit
    CPhI Milan
    Exhibiting
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothEurofins Assurance: Ensuring compliance, quality, and safety with expert inspection and certification.

    Sun Pharmaceutical

    Country : India

    City/Region : Dewas

    Audit Date : 2026-04-07

    Audit Type : On-Site

    Eurofins Assurance

    02

    Eurofins Assurance

    Belgium
    arrow
    Get Site Audit
    CPhI Milan
    Exhibiting
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothEurofins Assurance: Ensuring compliance, quality, and safety with expert inspection and certification.

    Alkaloida Chemical

    Country : Hungary

    City/Region : Tiszavasvari

    Audit Date : 2025-06-25

    Audit Type : On-Site

    Eurofins Assurance

    03

    Eurofins Assurance

    Belgium
    arrow
    Get Site Audit
    CPhI Milan
    Exhibiting
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothEurofins Assurance: Ensuring compliance, quality, and safety with expert inspection and certification.

    Sun Pharmaceutical

    Country : India

    City/Region : Dahej

    Audit Date : 2025-04-09

    Audit Type : On-Site

    Eurofins Assurance

    04

    Eurofins Assurance

    Belgium
    arrow
    Get Site Audit
    CPhI Milan
    Exhibiting
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothEurofins Assurance: Ensuring compliance, quality, and safety with expert inspection and certification.

    Alkaloida Chemical

    Country : Hungary

    City/Region : Tiszavasvari

    Audit Date : 2024-05-29

    Audit Type : On-Site

    Eurofins Assurance

    05

    Eurofins Assurance

    Belgium
    arrow
    Get Site Audit
    CPhI Milan
    Exhibiting
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothEurofins Assurance: Ensuring compliance, quality, and safety with expert inspection and certification.

    Sun Pharmaceutical

    Country : India

    City/Region : Bharuch

    Audit Date : 2024-05-15

    Audit Type : On-Site

    Eurofins Assurance

    06

    Eurofins Assurance

    Belgium
    arrow
    Get Site Audit
    CPhI Milan
    Exhibiting
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothEurofins Assurance: Ensuring compliance, quality, and safety with expert inspection and certification.

    Sun Pharmaceutical

    Country : India

    City/Region : Gujarat

    Audit Date : 2024-05-13

    Audit Type : On-Site

    Eurofins Assurance

    07

    Eurofins Assurance

    Belgium
    arrow
    Get Site Audit
    CPhI Milan
    Exhibiting
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothEurofins Assurance: Ensuring compliance, quality, and safety with expert inspection and certification.

    Sun Pharmaceutical

    Country : India

    City/Region : Dewas

    Audit Date : 2024-04-15

    Audit Type : On-Site

    Eurofins Assurance

    08

    AuditGMP Pharma

    Spain
    arrow
    Get Site Audit
    CPhI Milan
    Attending
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothAuditGMP Pharma SL delivers ISO 17020-accredited GMP audits and compliance services with expert, reliable, and tailored solutions.

    Sun Pharmaceutical Industries Europe B.V.

    Country : Netherlands

    City/Region : Hoofddorp

    Audit Date : Jun-25

    Audit Type : On-Site

    Company Banner

    09

    AuditGMP Pharma

    Spain
    arrow
    Get Site Audit
    CPhI Milan
    Attending
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothAuditGMP Pharma SL delivers ISO 17020-accredited GMP audits and compliance services with expert, reliable, and tailored solutions.

    Sun Pharmaceutical Industries Limited - Ahmednagar Site

    Country : India

    City/Region : Ahmedabad

    Audit Date : Jul-23

    Audit Type : On-Site

    Company Banner

    10

    AuditGMP Pharma

    Spain
    arrow
    Get Site Audit
    CPhI Milan
    Attending
    • fda
    • EDQM
    • WHO-GMP
    Virtual BoothAuditGMP Pharma SL delivers ISO 17020-accredited GMP audits and compliance services with expert, reliable, and tailored solutions.

    Sun Pharmaceutical Industries Limited - Village Toansa

    Country : India

    City/Region : Toansa Village, Nawanshahar District

    Audit Date : Feb-24

    Audit Type : On-Site

    Company Banner
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    ABOUT THIS PAGE

    Contact Sun Pharmaceutical Industries Limited and get a quotation

    Sun Pharmaceutical Industries Limited is a supplier offers 405 products (APIs, Excipients or Intermediates).

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