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01 1Ethypharm

02 12care4

03 1Abacus Medicine

04 1Altan Pharma

05 1As Kevelt

06 2Central Procurement & Supplies Unit

07 1Ebb Medical

08 7Endo International

09 2Ferring Pharmaceuticals

10 1Flagship Biotech International Pvt. Ltd

11 1Genex Pharma

12 1Hikma Pharmaceuticals

13 2Lifespan Biotech

14 2Meda Ab

15 3Medartuum

16 1Meitheal Pharmaceuticals

17 5ORIFARM GROUP AS

18 2Pfizer Consumer Healthcare

19 44Pfizer Inc

20 4Recordati

21 1S.C. Rompharm Company SRL

22 3The Simple Pharma Company Limited

23 22Viatris

24 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

VMX
Not Confirmed
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VMX
Not Confirmed

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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03

VMX
Not Confirmed
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VMX
Not Confirmed

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

VMX
Not Confirmed
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VMX
Not Confirmed

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

VMX
Not Confirmed
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VMX
Not Confirmed

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

VMX
Not Confirmed
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VMX
Not Confirmed

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

VMX
Not Confirmed
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VMX
Not Confirmed

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

VMX
Not Confirmed
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VMX
Not Confirmed

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

VMX
Not Confirmed
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VMX
Not Confirmed

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

VMX
Not Confirmed
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VMX
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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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11

VMX
Not Confirmed
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VMX
Not Confirmed

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

VMX
Not Confirmed
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VMX
Not Confirmed

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

VMX
Not Confirmed
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VMX
Not Confirmed

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

VMX
Not Confirmed
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VMX
Not Confirmed

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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15

VMX
Not Confirmed
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VMX
Not Confirmed

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

VMX
Not Confirmed
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VMX
Not Confirmed

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

VMX
Not Confirmed
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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

VMX
Not Confirmed
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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

VMX
Not Confirmed
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VMX
Not Confirmed

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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20

VMX
Not Confirmed
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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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