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    01

    EUROAPI

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    Virtual BoothEUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Dexamethasone Sodium Metasulfobenzoate; Framycetin Sulfate; Gramicidin

    Brand Name : Sofradex

    Dosage Form : Eye/Ear Drops

    Dosage Strength :

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    Approval Date : 09-12-1963

    Application Number : 1.96E+13

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    02

    Aspen Pharmacare Holdings

    South Africa
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    Regulatory Info : DISCN

    Registration Country : USA

    DEXAMETHASONE SODIUM PHOSPHATE

    Brand Name : HEXADROL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1982-01-01

    Application Number : 14694

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    Registration Country : USA

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    Dr. Reddy's Laboratories

    India
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    Regulatory Info : DISCN

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    DEXAMETHASONE SODIUM PHOSPHATE

    Brand Name : DEXAMETHASONE SODIUM PHOSPHATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4MG PHOSPHATE/ML

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    Approval Date : 1986-04-09

    Application Number : 89169

    Regulatory Info : DISCN

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    04

    Aspen Pharmacare Holdings

    South Africa
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    Regulatory Info : DISCN

    Registration Country : USA

    DEXAMETHASONE SODIUM PHOSPHATE

    Brand Name : HEXADROL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 14694

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Aspen Pharmacare Holdings

    South Africa
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    Regulatory Info : DISCN

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    DEXAMETHASONE SODIUM PHOSPHATE

    Brand Name : HEXADROL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 20MG PHOSPHATE/ML

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    Approval Date : 1982-01-01

    Application Number : 14694

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    06

    Aspen Pharmacare Holdings

    South Africa
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    Regulatory Info : Originator

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    Dexamethasone sodium phosphate

    Brand Name : Voxidex

    Dosage Form : EED

    Dosage Strength : 1mg/ml

    Packaging : 1X1mg/ml

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    Registration Country : South Africa

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    07

    Bausch & Lomb Incorporated

    Canada
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    DEXAMETHASONE SODIUM PHOSPHATE

    Brand Name : DEXAMETHASONE SODIUM PHOSPHATE

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC, OTIC

    Dosage Strength : EQ 0.1% PHOSPHATE

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    Approval Date : 1996-07-26

    Application Number : 40069

    Regulatory Info : RX

    Registration Country : USA

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    08

    Fresenius Kabi USA

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    Regulatory Info : RX

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    DEXAMETHASONE SODIUM PHOSPHATE

    Brand Name : DEXAMETHASONE SODIUM PHOSPHATE PRESERVATIVE FREE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10MG PHOSPHATE/ML

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    Approval Date : 2003-04-11

    Application Number : 40491

    Regulatory Info : RX

    Registration Country : USA

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    09

    Fresenius Kabi USA

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    Regulatory Info : RX

    Registration Country : USA

    DEXAMETHASONE SODIUM PHOSPHATE

    Brand Name : DEXAMETHASONE SODIUM PHOSPHATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10MG PHOSPHATE/ML

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    Approval Date : 2005-04-22

    Application Number : 40572

    Regulatory Info : RX

    Registration Country : USA

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    10

    Merck & Co

    U.S.A
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    Merck & Co

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    Regulatory Info : DISCN

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    DEXAMETHASONE SODIUM PHOSPHATE

    Brand Name : DECADRON

    Dosage Form : OINTMENT;OPHTHALMIC

    Dosage Strength : EQ 0.05% PHOSPHATE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11977

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Merck & Co

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    DEXAMETHASONE SODIUM PHOSPHATE

    Brand Name : DECADRON

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : EQ 0.1% PHOSPHATE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11983

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Merck & Co

    U.S.A
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    Regulatory Info : DISCN

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    DEXAMETHASONE SODIUM PHOSPHATE

    Brand Name : DECADRON

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC, OTIC

    Dosage Strength : EQ 0.1% PHOSPHATE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11984

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Merck & Co

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    DEXAMETHASONE SODIUM PHOSPHATE

    Brand Name : DECADRON

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 12071

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    Merck & Co

    U.S.A
    PEGS Boston Summit
    Not Confirmed
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    Regulatory Info : DISCN

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    DEXAMETHASONE SODIUM PHOSPHATE

    Brand Name : DECADRON

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 24MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 12071

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    Merck & Co

    U.S.A
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    Not Confirmed
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    Merck & Co

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    Regulatory Info : DISCN

    Registration Country : USA

    DEXAMETHASONE SODIUM PHOSPHATE; LIDOCAINE HYDROCHLORIDE

    Brand Name : DECADRON W/ XYLOCAINE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4MG PHOSPHATE/ML;10MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 13334

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    Merck & Co

    U.S.A
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    Not Confirmed
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    Merck & Co

    U.S.A
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    Regulatory Info : DISCN

    Registration Country : USA

    DEXAMETHASONE SODIUM PHOSPHATE; NEOMYCIN SULFATE

    Brand Name : NEODECADRON

    Dosage Form : SOLUTION/DROPS;OPHTHALMIC

    Dosage Strength : EQ 0.1% PHOSPHATE;EQ 3.5MG BASE/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 50322

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    UCB Pharma S.A

    Belgium
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    Not Confirmed
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    Belgium
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    Regulatory Info : DISCN

    Registration Country : USA

    DEXAMETHASONE SODIUM PHOSPHATE

    Brand Name : DEXACORT

    Dosage Form : AEROSOL, METERED;INHALATION

    Dosage Strength : EQ 0.1MG PHOSPHATE/INH

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 13413

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    UCB Pharma S.A

    Belgium
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    Belgium
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    Regulatory Info : DISCN

    Registration Country : USA

    DEXAMETHASONE SODIUM PHOSPHATE

    Brand Name : DEXACORT

    Dosage Form : AEROSOL;NASAL

    Dosage Strength : EQ 0.1MG PHOSPHATE/INH

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 14242

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    Viatris

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    Regulatory Info : RX

    Registration Country : USA

    DEXAMETHASONE SODIUM PHOSPHATE

    Brand Name : DEXAMETHASONE SODIUM PHOSPHATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 10MG PHOSPHATE/ML

    Packaging :

    Approval Date : 2008-08-29

    Application Number : 40802

    Regulatory Info : RX

    Registration Country : USA

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    20

    Viatris

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    DEXAMETHASONE SODIUM PHOSPHATE

    Brand Name : DEXAMETHASONE SODIUM PHOSPHATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 4MG PHOSPHATE/ML

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    Approval Date : 2008-08-29

    Application Number : 40803

    Regulatory Info : RX

    Registration Country : USA

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