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CPhI India 2024CPhI India 2024
Industry Trade Show
Not Confirmed
26-28 November, 2024
Saudi International Ex...Saudi International Expo
Industry Trade Show
Not Confirmed
28-30 October, 2024
SupplySide West 2024SupplySide West 2024
Industry Trade Show
Not Confirmed
28 October-01 November, 2024
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INTERVIEW #SpeakPharma
[Sponsored by another company]https://www.pharmacompass.com/speak-pharma/due-to-its-20-year-mastery-in-micronization-inke-has-emerged-a-cornerstone-in-treating-global-respiratory-diseases
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22 Jul 2024
// FDA
https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=216456
23 Apr 2024
// Blake Brittain REUTERS
https://www.reuters.com/legal/us-supreme-court-rejects-vanda-pharmaceuticals-case-over-sleep-drug-patents-2024-04-22/
30 Mar 2024
// Fraiser Kansteiner FIERCE PHARMA
https://www.fiercepharma.com/pharma/teva-follows-suit-after-hikmas-2023-complaint-arguing-amarin-locked-drug-ingredient-supply
01 Feb 2024
// Kevin Dunleavy FIERCE PHARMA
https://www.fiercepharma.com/pharma/continuing-its-transformation-teva-confirms-intent-sell-api-business
25 Dec 2021
// TIMESOFISRAEL
https://www.timesofisrael.com/accused-of-complicity-in-opioid-crisis-teva-launches-nasal-spray-to-treat-overdose/
09 Sep 2021
// N. H. Dunn FIERCEPHARMA
https://www.fiercepharma.com/pharma/teva-trailing-cgrp-rivals-migraine-can-t-find-a-win-ajovy-analysis-versus-biohaven-and
JDMF
Registration Number : 228MF10057
Registrant's Address : Neot-Hovav Eco-Industrial Park, Emek Sara P. O. Box 2049 Be'er Sheva 8412316, Israel
Initial Date of Registration : 2016-02-18
Latest Date of Registration : 2016-02-18
Registration Number : 224MF10142
Registrant's Address : Neot-Hovav Eco-Industrial Park, Emek Sara P. O. Box 2049 Be'er Sheva 8412316, Israel
Initial Date of Registration : 2012-07-31
Latest Date of Registration : 2012-07-31
JDMF
Registration Number : 225MF10130
Registrant's Address : Neot-Hovav Eco-Industrial Park, Emek Sara P. O. Box 2049 Be'er Sheva 8412316, Israel
Initial Date of Registration : 2013-07-09
Latest Date of Registration : 2013-07-09
Registration Number : 302MF10024
Registrant's Address : Neot-Hovav Eco-Industrial Park, Emek Sara P. O. Box 2049 Be'er Sheva 8412316, Israel
Initial Date of Registration : 2020-02-06
Latest Date of Registration : 2020-02-06
JDMF
Registration Number : 219MF10026
Registrant's Address : Neot-Hovav Eco-Industrial Park, Emek Sara P. O. Box 2049 Be'er Sheva 8412316, Israel
Initial Date of Registration : 2007-02-05
Latest Date of Registration : 2022-04-06
JDMF
Registration Number : 218MF10535
Registrant's Address : Neot-Hovav Eco-Industrial Park, Emek Sara P. O. Box 2049 Be'er Sheva 8412316, Israel
Initial Date of Registration : 2006-06-01
Latest Date of Registration : 2024-08-22
Registration Number : 219MF10151
Registrant's Address : Neot-Hovav Eco-Industrial Park, Emek Sara P. O. Box 2049 Be'er Sheva 8412316, Israel
Initial Date of Registration : 2007-04-27
Latest Date of Registration : 2007-04-27
JDMF
Registration Number : 226MF10176
Registrant's Address : Neot-Hovav Eco-Industrial Park, Emek Sara P. O. Box 2049 Be'er Sheva 8412316, Israel
Initial Date of Registration : 2014-09-01
Latest Date of Registration : 2014-09-01
JDMF
Registration Number : 227MF10270
Registrant's Address : Neot-Hovav Eco-Industrial Park, Emek Sara P. O. Box 2049 Be'er Sheva 8412316, Israel
Initial Date of Registration : 2015-11-19
Latest Date of Registration : 2023-07-19
JDMF
Registration Number : 223MF10114
Registrant's Address : Neot-Hovav Eco-Industrial Park, Emek Sara P. O. Box 2049 Be'er Sheva 8412316, Israel
Initial Date of Registration : 2011-07-25
Latest Date of Registration : 2012-05-15
Details:
AUSTEDO (deutetrabenazine) is the first and only vesicular monoamine transporter 2 (VMAT2) inhibitor approved by the U.S. Food and Drug Administration for the treatment of tardive dyskinesia (TD) in adults and for the treatment of chorea associated with Huntington’s disease.
Lead Product(s): Deutetrabenazine
Therapeutic Area: Musculoskeletal Brand Name: Austedo
Study Phase: Phase IIIProduct Type: Small molecule
Sponsor: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable October 18, 2022
Lead Product(s) : Deutetrabenazine
Therapeutic Area : Musculoskeletal
Highest Development Status : Phase III
Partner/Sponsor/Collaborator : Not Applicable
Deal Size : Not Applicable
Deal Type : Not Applicable
Teva Announces Results from 3-Year Study Assessing the Safety and Tolerability of AUSTEDO® (deute...
Details : AUSTEDO (deutetrabenazine) is the first and only vesicular monoamine transporter 2 (VMAT2) inhibitor approved by the U.S. Food and Drug Administration for the treatment of tardive dyskinesia (TD) in adults and for the treatment of chorea associated with ...
Brand Name : Austedo
Molecule Type : Small molecule
Upfront Cash : Not Applicable
October 18, 2022
Details:
mdc-IRM, (risperidone) extended-release injectable suspension for the treatment of patients with schizophrenia (Teva codename: TV-46000), is the most advanced investigational product based on MedinCell’s BEPO® technology.
Lead Product(s): Risperidone
Therapeutic Area: Psychiatry/Psychology Brand Name: mdc-IRM
Study Phase: Phase IIIProduct Type: Small molecule
Recipient: MedinCell
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable May 03, 2022
Lead Product(s) : Risperidone
Therapeutic Area : Psychiatry/Psychology
Highest Development Status : Phase III
Recipient : MedinCell
Deal Size : Not Applicable
Deal Type : Not Applicable
MedinCell’s Partner Teva Provides Additional Information Regarding the New Drug Application for ...
Details : mdc-IRM, (risperidone) extended-release injectable suspension for the treatment of patients with schizophrenia (Teva codename: TV-46000), is the most advanced investigational product based on MedinCell’s BEPO® technology.
Brand Name : mdc-IRM
Molecule Type : Small molecule
Upfront Cash : Not Applicable
May 03, 2022
Regulatory Info :
Registration Country : Norway
Dosage Form : Inhalation liquid for ne...
Brand Name : Budesonide Teva
Dosage Strength : 0.5 mg/ml
Packaging : ampoule 20 2ml
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Inhalation liquid for ne...
Brand Name : Budesonide Teva
Dosage Strength : 0.25 mg/ml
Packaging : ampoule 20 2ml
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Dosage Form : Inhalation liquid for ne...
Brand Name : Budesonide Teva
Dosage Strength : 0.125 mg/ml
Packaging : ampoule 20 2ml
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Budesonide, Formoterol Fumarate Dihydrate
Dosage Form : Inhalation powder
Brand Name : DuoResp Spiromax
Dosage Strength : 320 microg/9 microg
Packaging : Inhaler 1 60doses
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Budesonide, Formoterol Fumarate Dihydrate
Dosage Form : Inhalation powder
Brand Name : DuoResp Spiromax
Dosage Strength : 320 microg/9 microg
Packaging : Inhaler 3 60doses
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Budesonide, Formoterol Fumarate Dihydrate
Dosage Form : Inhalation powder
Brand Name : DuoResp Spiromax
Dosage Strength : 160 microg/4.5 microg
Packaging : Inhaler 3 120doses
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : Norway
Budesonide, Formoterol Fumarate Dihydrate
Dosage Form : Inhalation powder
Brand Name : DuoResp Spiromax
Dosage Strength : 160 microg/4.5 microg
Packaging : Inhaler 1 120doses
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : CABOZANTINIB
Dosage Strength : 20MG
Packaging :
Approval Date :
Application Number : 215942
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : CABOZANTINIB
Dosage Strength : 60MG
Packaging :
Approval Date :
Application Number : 215942
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : CABOZANTINIB
Dosage Strength : 40MG
Packaging :
Approval Date :
Application Number : 215942
Regulatory Info :
Registration Country : USA
Inspections and registrations
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Assia Chemical Industries Ltd is a supplier offers 22 products (APIs, Excipients or Intermediates).
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