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List of All Manufacturers & Suppliers of Alprox-TD Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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$ API Ref.Price (USD/KG) : 880,645Xls
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01 1Ethypharm

02 7ENDO OPERATIONS

03 1Ferring Pharmaceuticals

04 1Flagship Biotech International Pvt. Ltd

05 1Hikma Pharmaceuticals

06 2Lifespan Biotech

07 6Meda - Asker

08 4Meda AB

09 1Meitheal Pharmaceuticals

10 1ORIFARM GROUP AS

11 2Pfizer Consumer Healthcare

12 38Pfizer Inc

13 2Recordati

14 4Sandoz B2B

15 4Viatris

16 2Xian Libang Pharmaceutical Co.,Ltd

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEthypharm is an international Pharma company with European roots manufacturing and commercializing essential drugs all over the world.

Regulatory Info :

Registration Country : France

Alprostadil

Brand Name :

Dosage Form : Powder for Solution for Infusion

Dosage Strength : 20MCG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : France

Ethypharm

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ALPROSTADIL

Brand Name : PROSTIN VR PEDIATRIC

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.5MG/ML

Packaging :

Approval Date : 1982-01-01

Application Number : 18484

Regulatory Info : RX

Registration Country : USA

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ALPROSTADIL

Brand Name : CAVERJECT

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.01MG/VIAL

Packaging :

Approval Date : 1995-07-06

Application Number : 20379

Regulatory Info : RX

Registration Country : USA

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ALPROSTADIL

Brand Name : CAVERJECT

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.02MG/VIAL

Packaging :

Approval Date : 1995-07-06

Application Number : 20379

Regulatory Info : RX

Registration Country : USA

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ALPROSTADIL

Brand Name : CAVERJECT

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.005MG/VIAL

Packaging :

Approval Date : 1996-06-27

Application Number : 20379

Regulatory Info : DISCN

Registration Country : USA

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ALPROSTADIL

Brand Name : CAVERJECT

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.04MG/VIAL

Packaging :

Approval Date : 1997-05-19

Application Number : 20379

Regulatory Info : RX

Registration Country : USA

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ALPROSTADIL

Brand Name : CAVERJECT

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.005MG/ML

Packaging :

Approval Date : 1997-10-31

Application Number : 20755

Regulatory Info : DISCN

Registration Country : USA

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ALPROSTADIL

Brand Name : CAVERJECT

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.01MG/ML

Packaging :

Approval Date : 1997-10-01

Application Number : 20755

Regulatory Info : DISCN

Registration Country : USA

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ALPROSTADIL

Brand Name : CAVERJECT

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.02MG/ML

Packaging :

Approval Date : 1997-10-01

Application Number : 20755

Regulatory Info : DISCN

Registration Country : USA

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ALPROSTADIL

Brand Name : MUSE

Dosage Form : SUPPOSITORY;URETHRAL

Dosage Strength : 0.125MG

Packaging :

Approval Date : 1996-11-19

Application Number : 20700

Regulatory Info : DISCN

Registration Country : USA

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ALPROSTADIL

Brand Name : MUSE

Dosage Form : SUPPOSITORY;URETHRAL

Dosage Strength : 0.25MG

Packaging :

Approval Date : 1996-11-19

Application Number : 20700

Regulatory Info : DISCN

Registration Country : USA

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ALPROSTADIL

Brand Name : MUSE

Dosage Form : SUPPOSITORY;URETHRAL

Dosage Strength : 0.5MG

Packaging :

Approval Date : 1996-11-19

Application Number : 20700

Regulatory Info : DISCN

Registration Country : USA

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ALPROSTADIL

Brand Name : MUSE

Dosage Form : SUPPOSITORY;URETHRAL

Dosage Strength : 1MG

Packaging :

Approval Date : 1996-11-19

Application Number : 20700

Regulatory Info : DISCN

Registration Country : USA

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ENDO OPERATIONS

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ALPROSTADIL

Brand Name : EDEX

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.005MG/VIAL

Packaging :

Approval Date : 1997-06-12

Application Number : 20649

Regulatory Info : DISCN

Registration Country : USA

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ENDO OPERATIONS

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ALPROSTADIL

Brand Name : EDEX

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.01MG/VIAL

Packaging :

Approval Date : 1997-06-12

Application Number : 20649

Regulatory Info : RX

Registration Country : USA

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ENDO OPERATIONS

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ALPROSTADIL

Brand Name : EDEX

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.02MG/VIAL

Packaging :

Approval Date : 1997-06-12

Application Number : 20649

Regulatory Info : RX

Registration Country : USA

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ENDO OPERATIONS

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ALPROSTADIL

Brand Name : EDEX

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.04MG/VIAL

Packaging :

Approval Date : 1997-06-12

Application Number : 20649

Regulatory Info : RX

Registration Country : USA

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ENDO OPERATIONS

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ALPROSTADIL

Brand Name : EDEX

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.01MG/VIAL

Packaging :

Approval Date : 1998-07-30

Application Number : 20649

Regulatory Info : RX

Registration Country : USA

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ENDO OPERATIONS

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ALPROSTADIL

Brand Name : EDEX

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.02MG/VIAL

Packaging :

Approval Date : 1998-07-30

Application Number : 20649

Regulatory Info : RX

Registration Country : USA

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ENDO OPERATIONS

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ALPROSTADIL

Brand Name : EDEX

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 0.04MG/VIAL

Packaging :

Approval Date : 1998-07-30

Application Number : 20649

Regulatory Info : RX

Registration Country : USA

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