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01 1Ethypharm

02 7Endo International

03 1Ferring Pharmaceuticals

04 1Flagship Biotech International Pvt. Ltd

05 1Hikma Pharmaceuticals

06 2Lifespan Biotech

07 6Meda - Asker

08 1Meitheal Pharmaceuticals

09 1ORIFARM GROUP AS

10 2Pfizer Consumer Healthcare

11 28Pfizer Inc

12 2Recordati

13 4Viatris

14 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

02

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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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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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04

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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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05

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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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06

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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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07

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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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08

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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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09

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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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10

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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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12

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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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13

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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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14

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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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16

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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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17

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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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18

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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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19

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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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