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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

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    Dexamethasone Sodium Metasulfobenzoate; Framycetin Sulfate; Gramicidin

    Brand Name : Sofradex

    Dosage Form : Eye/Ear Drops

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    Approval Date : 09/12/1963

    Application Number : 19631209000027

    Regulatory Info : Deregistered

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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    Dosage Strength : EQ 4MG PHOSPHATE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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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    03

    Dr. Reddy's Laboratories

    India
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    Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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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

    Registration Country : USA

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    Pharmathen SA

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    Virtual BoothPharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.

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    Regulatory Info : Approved

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    Dexamethasone Sodium Phosphate (also known as Dexamethasone 21-phosphate or Dexamethasone Dihydrogen Phosphate)

    Brand Name : Oratoria

    Dosage Form : Eye Drop

    Dosage Strength : 1mg/ml

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    Approval Date : 09/02/2018

    Application Number : 20161219000022

    Regulatory Info : Approved

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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 10MG 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

    Regulatory Info : DISCN

    Registration Country : USA

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    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

    Regulatory Info : DISCN

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    Aspen Pharmacare Holdings

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    Regulatory Info : Originator

    Registration Country : South Africa

    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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    Bausch & Lomb Incorporated

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    Regulatory Info : RX

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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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    09

    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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    10

    Fresenius Kabi USA

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    Regulatory Info : RX

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    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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    11

    Merck & Co

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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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    12

    Merck & Co

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    Regulatory Info : DISCN

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    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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    Merck & Co

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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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    Merck & Co

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    Regulatory Info : DISCN

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    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**

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    Approval Date : 1982-01-01

    Application Number : 12071

    Regulatory Info : DISCN

    Registration Country : USA

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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 : INJECTABLE;INJECTION

    Dosage Strength : EQ 24MG 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 : 12071

    Regulatory Info : DISCN

    Registration Country : USA

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    Merck & Co

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    Regulatory Info : DISCN

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    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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    UCB Pharma S.A

    Belgium
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    Regulatory Info : DISCN

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    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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    UCB Pharma S.A

    Belgium
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    Regulatory Info : DISCN

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    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

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    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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    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

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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.