Ethypharm is an international Pharma company with European roots manufacturing and commercializing essential drugs all over the world.
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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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01 1Alprostadil 10Mcg 1 Units Use Intracavernoso
02 1Alprostadil 20Mcg 1 Unit Parenteral Use
03 1Alprostadil 500Mcg 1Ml 1 Units Parenteral Use
04 1Alprostadil 60Mcg 1 Unit Parenteral Use
05 1Concentrate for infusion solution, solution
06 1Concentrate to the infusion fluid, resolution
07 1Cream
08 1INJ
09 19INJECTABLE;INJECTION
10 2Injectable Emulsion
11 3Injection
12 6Intraurethral
13 1KIT
14 1POI
15 1POWDER FOR SOLUTION
16 3Powder and liquid to the injection fluid, resolution
17 1Powder for Solution for Infusion
18 1SOLUTION
19 4SUPPOSITORY;URETHRAL
20 9Blank
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01 9DISCN
02 1Generic
03 2Originator
04 14RX
05 33Blank
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01 2ALPROSTADIL
02 2Alprostar
03 6Bondil
04 7CAVERJECT
05 2CAVERJECT IMPULSE
06 1CAVERJECT STERILE POWDER
07 1CAVERJECT STERILE POWDER - PWS 23.2MCG/VIAL
08 8Caverject
09 1Caverject 20ug
10 3Caverject Dual
11 2Caverject Impulse
12 7EDEX
13 4MUSE
14 1PROSTIN VR PEDIATRIC
15 1PROSTIN VR STERILE SOLUTION
16 1Prostin VR
17 1Prostin Vr
18 1Prostitutes
19 1Prostivas
20 1Vitaros
21 6Blank
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01 2Australia
02 3Canada
03 2China
04 1France
05 3India
06 11Italy
07 12Norway
08 2South Africa
09 23USA
Ethypharm is an international Pharma company with European roots manufacturing and commercializing essential drugs all over the world.
Regulatory Info :
Registration Country : France
Brand Name :
Dosage Form : Powder for Solution for Infusion
Dosage Strength : 20MCG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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