Ethypharm is an international Pharma company with European roots manufacturing and commercializing essential drugs all over the world.
01 1Ethypharm
02 7Endo International
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
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 2CREAM
06 1Concentrate for infusion solution, solution
07 1Concentrate to the infusion fluid, resolution
08 1Cream
09 2Dry Sub
10 1INJ
11 19INJECTABLE;INJECTION
12 2Injectable Emulsion
13 3Injection
14 6Intraurethral
15 1KIT
16 1KONCENTRAT TILL INFUSIONSVÄTSKA, LÖSNING
17 2KRÄM
18 1POI
19 6POWDER AND SOLVENT FOR SOLUTION FOR INJECTION
20 1POWDER FOR SOLUTION
21 3Powder and liquid to the injection fluid, resolution
22 1Powder for Solution for Infusion
23 1SOLUTION
24 4SUPPOSITORY;URETHRAL
25 1Trockensub
26 4URETRALSTIFT
27 9Blank
01 9DISCN
02 1Generic
03 2Originator
04 14RX
05 51Blank
01 2ALPROSTADIL
02 2Alprostar
03 10Bondil
04 7CAVERJECT
05 2CAVERJECT IMPULSE
06 1CAVERJECT STERILE POWDER
07 1CAVERJECT STERILE POWDER - PWS 23.2MCG/VIAL
08 15Caverject
09 1Caverject 20ug
10 2Caverject DC
11 3Caverject Dual
12 2Caverject Impulse
13 7EDEX
14 2Eafelb
15 4MUSE
16 1PROSTIN VR PEDIATRIC
17 1PROSTIN VR STERILE SOLUTION
18 1Prostin VR
19 1Prostin Vr
20 1Prostitutes
21 2Prostivas
22 3Vitaros
23 6Blank
01 2Australia
02 3Canada
03 2China
04 1France
05 3India
06 11Italy
07 12Norway
08 2South Africa
09 15Sweden
10 3Switzerland
11 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
