04 Oct 2024
// PRESS RELEASE
17 Jun 2024
// PRESS RELEASE
13 Jun 2024
// PRESS RELEASE
Ethypharm is an international Pharma company with European roots manufacturing and commercializing essential drugs all over the world.
About
Industry Trade Show
Not Confirmed
24-26 June, 2025
CPhI WW FrankfurtCPhI WW Frankfurt
Industry Trade Show
Booth #5.0D100
28-30 October, 2025
Industry Trade Show
Not Confirmed
15-19 June, 2025
CONTACT DETAILS
Events
Webinars & Exhibitions
Industry Trade Show
Not Confirmed
24-26 June, 2025
CPhI WW FrankfurtCPhI WW Frankfurt
Industry Trade Show
Booth #5.0D100
28-30 October, 2025
Industry Trade Show
Not Confirmed
15-19 June, 2025
CORPORATE CONTENT #SupplierSpotlight
04 Oct 2024
// PRESS RELEASE
https://www.ethypharm.com/blog/newsroom/ethypharm-announces-the-appointment-of-eric-chevalier-as-group-human-resources-director/
17 Jun 2024
// PRESS RELEASE
https://www.ethypharm.com/wp-content/uploads/2024/06/18-06-24-Press-Release-Argatroban-Ethypharm-Final.pdf
13 Jun 2024
// PRESS RELEASE
https://www.ethypharm.com/wp-content/uploads/2024/06/13062024_Group-PR_-Ethypharm-Expands-its-Mesalazine-Portfolio-in-China_FINAL-PR-NEWSWIRE.pdf
06 Apr 2024
// PRESS RELEASE
https://www.ethypharm.com/wp-content/uploads/2022/10/Agreement-Gaia-AG-EN.pdf
13 Jun 2023
// PRESS RELEASE
https://www.ethypharm.com/wp-content/uploads/2023/06/PR-Xavier-LASSERRE-appointed_CCO_Ethypharm-final.pdf
01 May 2023
// PRESS RELEASE
https://www.ethypharm.com/wp-content/uploads/2023/05/Aurora_Ethypharm_Extension-Pilot-Program_FINAL-1.pdf
RLD : No
TE Code : AB
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : BUPRENORPHINE HYDROCHLOR...
Dosage Strength : EQ 2MG BASE
Approval Date : 2010-09-24
Application Number : 90622
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : BUPRENORPHINE HYDROCHLOR...
Dosage Strength : EQ 8MG BASE
Approval Date : 2010-09-24
Application Number : 90622
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : BUPRENORPHINE HYDROCHLOR...
Dosage Strength : EQ 2MG BASE;EQ 0.5MG BAS...
Approval Date : 2015-10-16
Application Number : 204431
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE
Dosage Form : TABLET; SUBLINGUAL
Proprietary Name : BUPRENORPHINE HYDROCHLOR...
Dosage Strength : EQ 8MG BASE;EQ 2MG BASE
Approval Date : 2015-10-16
Application Number : 204431
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : CAPSULE, DELAYED REL PELLETS; ...
Proprietary Name : ESOMEPRAZOLE MAGNESIUM
Dosage Strength : EQ 20MG BASE
Approval Date : 2021-03-31
Application Number : 90841
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Dosage Form : CAPSULE, DELAYED REL PELLETS; ...
Proprietary Name : ESOMEPRAZOLE MAGNESIUM
Dosage Strength : EQ 40MG BASE
Approval Date : 2021-03-31
Application Number : 90841
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
Regulatory Info :
Registration Country : Norway
Dosage Form : Solution for injection
Dosage Strength : 0.1mg/ml
Packaging : Ampoule av glass ...
Brand Name : Adrenalin Martindale Pharma
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Solution for injection
Dosage Strength : 1mg/ml
Packaging : Ampoule av glass ...
Brand Name : Adrenalin Ethypharm
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Lyofilisattablett
Dosage Strength : 8 mg
Packaging : Endose blister pa...
Brand Name : Espranor
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Lyofilisattablett
Dosage Strength : 2 mg
Packaging : Endose blister pa...
Brand Name : Espranor
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Italy
Dosage Form : Extended Release Hard Capsules
Dosage Strength : 10 mg
Packaging : 16 UNITS 10 MG - O...
Brand Name : TWICE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Extended Release Hard Capsules
Dosage Strength : 100 mg
Packaging : 16 UNITS 100 MG - ...
Brand Name : TWICE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Extended Release Hard Capsules
Dosage Strength : 30 mg
Packaging : 16 UNITS 30 MG - O...
Brand Name : TWICE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Italy
Dosage Form : Extended Release Hard Capsules
Dosage Strength : 60 mg
Packaging : 16 UNITS 60 MG - O...
Brand Name : TWICE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : SOLUTION
Dosage Strength : 25MG/5ML
Packaging :
Brand Name : NOYADA
Approval Date :
Application Number : 2543915
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Dosage Form : SOLUTION
Dosage Strength : 5MG/5ML
Packaging :
Brand Name : NOYADA
Approval Date :
Application Number : 2543907
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Dosage Form : CAPSULE (EXTENDED RELEASE)
Dosage Strength : 15MG
Packaging : 20/50
Brand Name : M-ESLON
Approval Date :
Application Number : 2177749
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Dosage Form : CAPSULE (EXTENDED RELEASE)
Dosage Strength : 200MG
Packaging : 20/50
Brand Name : M-ESLON
Approval Date :
Application Number : 2177757
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Dosage Form : CAPSULE (EXTENDED RELEASE)
Dosage Strength : 30MG
Packaging : 20/50
Brand Name : M-ESLON
Approval Date :
Application Number : 2019949
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Dosage Form : CAPSULE (EXTENDED RELEASE)
Dosage Strength : 100MG
Packaging : 20/50
Brand Name : M-ESLON
Approval Date :
Application Number : 2019965
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Dosage Form : CAPSULE (EXTENDED RELEASE)
Dosage Strength : 60MG
Packaging : 20/50
Brand Name : M-ESLON
Approval Date :
Application Number : 2019957
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Dosage Form : CAPSULE (EXTENDED RELEASE)
Dosage Strength : 10MG
Packaging : 20/50
Brand Name : M-ESLON
Approval Date :
Application Number : 2019930
Regulatory Info : Narcotic (CDSA I)
Registration Country : Canada
Regulatory Info :
Registration Country : France
Dosage Form : Ampoule
Brand Name :
Dosage Strength : 200MG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Vial
Brand Name :
Dosage Strength : 250MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Ampoule
Brand Name :
Dosage Strength : 1MG/1ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Pre-filled Syringe
Brand Name :
Dosage Strength : 1MG/10ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Powder for Solution for Infu...
Brand Name :
Dosage Strength : 20MCG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Capsule
Brand Name :
Dosage Strength : 80MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Capsule
Brand Name :
Dosage Strength : 125MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Vial
Brand Name :
Dosage Strength : 37.5MG/5ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Ampoule
Brand Name :
Dosage Strength : 6.75MG/0.9ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Dosage Form : Ampoule
Brand Name :
Dosage Strength : 600MCG/ML
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Services
Packaging
Drug Product Manufacturing
API & Drug Product Development
Inspections and registrations
ABOUT THIS PAGE
Ethypharm is a supplier offers 2 products (APIs, Excipients or Intermediates).
Find a price of Esomeprazole Magnesium bulk offered by Ethypharm
Find a price of Fenofibrate bulk offered by Ethypharm