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    Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.

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    Boai NKY Pharmaceuticals Ltd. is one of the largest global PVP suppliers.

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    pharmacompass-1-m-2026-04-20

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    Nanjing Well is focused on R&D, production & sales of Pharmaceutical Excipients & Synthetic Lubricating base oils.

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    Ever Pharma, highly specialized CDMO in producing complex injectables including high potency & controlled substances, suspensions, etc.

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    01 1ALCON PHARMA

    02 1ALCON PHARMS LTD

    03 1APOTEX INC

    04 3BAUSCH AND LOMB

    05 1JOHNSON JOHNSON VISN

    06 1SENTISS

    07 1UNICHEM

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    01

    ALCON PHARMA

    U.S.A
    PEGS Boston Summit
    Not Confirmed
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    ALCON PHARMA

    U.S.A
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    PEGS Boston Summit
    Not Confirmed
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    RLD : Yes

    TE Code :

    KETOTIFEN FUMARATE

    Brand Name : ZADITOR

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.025% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 2006-10-19

    Application Number : 21066

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    02

    ALCON PHARMS LTD

    U.S.A
    PEGS Boston Summit
    Not Confirmed
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    ALCON PHARMS LTD

    U.S.A
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    PEGS Boston Summit
    Not Confirmed
    • fda
    • EDQM
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    RLD : No

    TE Code :

    KETOTIFEN FUMARATE

    Brand Name : ZADITOR

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.025% BASE

    Approval Date : 2008-09-02

    Application Number : 77200

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    03

    APOTEX INC

    Canada
    PEGS Boston Summit
    Not Confirmed
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    APOTEX INC

    Canada
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    PEGS Boston Summit
    Not Confirmed
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    RLD : No

    TE Code :

    KETOTIFEN FUMARATE

    Brand Name : KETOTIFEN FUMARATE

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.025% BASE

    Approval Date : 2006-05-09

    Application Number : 77354

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    BAUSCH AND LOMB

    Canada
    PEGS Boston Summit
    Not Confirmed
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    BAUSCH AND LOMB

    Canada
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    PEGS Boston Summit
    Not Confirmed
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    RLD : Yes

    TE Code :

    KETOTIFEN FUMARATE

    Brand Name : ALAWAY

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.025% BASE

    Approval Date : 2006-12-01

    Application Number : 21996

    RX/OTC/DISCN : OTC

    RLD : Yes

    TE Code :

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    05

    BAUSCH AND LOMB

    Canada
    PEGS Boston Summit
    Not Confirmed
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    BAUSCH AND LOMB

    Canada
    arrow
    PEGS Boston Summit
    Not Confirmed
    • fda
    • EDQM
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    RLD : Yes

    TE Code :

    KETOTIFEN FUMARATE

    Brand Name : CHILDRENS ALAWAY

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.025% BASE

    Approval Date : 2015-02-11

    Application Number : 21996

    RX/OTC/DISCN : OTC

    RLD : Yes

    TE Code :

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    06

    BAUSCH AND LOMB

    Canada
    PEGS Boston Summit
    Not Confirmed
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    BAUSCH AND LOMB

    Canada
    arrow
    PEGS Boston Summit
    Not Confirmed
    • fda
    • EDQM
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    RLD : No

    TE Code :

    KETOTIFEN FUMARATE

    Brand Name : ALAWAY

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.025% BASE

    Approval Date : 2020-09-24

    Application Number : 208158

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    JOHNSON JOHNSON VISN

    U.S.A
    PEGS Boston Summit
    Not Confirmed
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    JOHNSON JOHNSON VISN

    U.S.A
    arrow
    PEGS Boston Summit
    Not Confirmed
    • fda
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    RLD : Yes

    TE Code :

    KETOTIFEN FUMARATE

    Brand Name : ACUVUE THERAVISION WITH KETOTIFEN

    Dosage Form : DRUG-ELUTING CONTACT LENS;OPHTHALMIC

    Dosage Strength : EQ 19MCG BASE

    Approval Date : 2022-02-25

    Application Number : 22388

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    08

    SENTISS

    India
    PEGS Boston Summit
    Not Confirmed
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    SENTISS

    India
    arrow
    PEGS Boston Summit
    Not Confirmed
    • fda
    • EDQM
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    RLD : No

    TE Code :

    KETOTIFEN FUMARATE

    Brand Name : KETOTIFEN FUMARATE

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.025% BASE

    Approval Date : 2007-07-26

    Application Number : 77958

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    09

    UNICHEM

    U.S.A
    PEGS Boston Summit
    Not Confirmed
    arrow

    UNICHEM

    U.S.A
    arrow
    PEGS Boston Summit
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : No

    TE Code :

    KETOTIFEN FUMARATE

    Brand Name : KETOTIFEN FUMARATE

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.025% BASE

    Approval Date : 2020-06-01

    Application Number : 204059

    RX/OTC/DISCN : OTC

    RLD : No

    TE Code :

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.