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23 Apr 2021
// PRESS RELEASE
https://ecipharma.com/2021/04/23/eci-pharmaceuticals-llc-enters-into-exclusive-u-s-distribution-agreement-for-ibuprofen/
13 Nov 2018
// FDA
https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=210562
Details:
According to IQVIA data for the 12 months ended December 2020, total U.S. generic sales of Ibuprofen tablets 400 mg, 600 mg, 800 mg was approximately $110 million. Generic Folic Acid tablets 1 mg were approximately $20 million for the same period.
Lead Product(s): Ibuprofen
Therapeutic Area: Neurology Brand Name: Ibuprofen-Generic
Study Phase: ApprovedProduct Type: Small molecule
Sponsor: ECI Pharmaceuticals LLC
Deal Size: Undisclosed Upfront Cash: Undisclosed
Deal Type: Agreement April 23, 2021
Lead Product(s) : Ibuprofen
Therapeutic Area : Neurology
Highest Development Status : Approved
Partner/Sponsor/Collaborator : ECI Pharmaceuticals LLC
Deal Size : Undisclosed
Deal Type : Agreement
ECI Pharmaceuticals LLC Enters into Exclusive U.S. Distribution Agreement for Ibuprofen
Details : According to IQVIA data for the 12 months ended December 2020, total U.S. generic sales of Ibuprofen tablets 400 mg, 600 mg, 800 mg was approximately $110 million. Generic Folic Acid tablets 1 mg were approximately $20 million for the same period.
Brand Name : Ibuprofen-Generic
Molecule Type : Small molecule
Upfront Cash : Undisclosed
April 23, 2021
Regulatory Info : DISCN
Registration Country : USA
ALBUTEROL SULFATE; IPRATROPIUM BROMIDE
Dosage Form : SOLUTION;INHALATION
Brand Name : ALBUTEROL SULFATE AND IPR...
Dosage Strength : EQ 0.083% BASE;0.017%
Packaging :
Approval Date : 2006-12-21
Application Number : 76867
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : ALLOPURINOL
Dosage Strength : 100MG
Packaging :
Approval Date : 1985-12-31
Application Number : 70268
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMITRIPTYLINE HYDROCHLORI...
Dosage Strength : 25MG
Packaging :
Approval Date : 2020-04-07
Application Number : 212654
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMITRIPTYLINE HYDROCHLORI...
Dosage Strength : 50MG
Packaging :
Approval Date : 2021-09-29
Application Number : 212654
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMITRIPTYLINE HYDROCHLORI...
Dosage Strength : 100MG
Packaging :
Approval Date : 2021-09-29
Application Number : 212654
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMITRIPTYLINE HYDROCHLORI...
Dosage Strength : 10MG
Packaging :
Approval Date : 2021-09-29
Application Number : 212654
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMITRIPTYLINE HYDROCHLORI...
Dosage Strength : 75MG
Packaging :
Approval Date : 2021-09-29
Application Number : 212654
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : AMITRIPTYLINE HYDROCHLORI...
Dosage Strength : 150MG
Packaging :
Approval Date : 2021-09-29
Application Number : 212654
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : SOLUTION;INHALATION
Brand Name : ARFORMOTEROL TARTRATE
Dosage Strength : EQ 0.015MG BASE/2ML
Packaging :
Approval Date : 2024-04-02
Application Number : 214901
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BENZTROPINE MESYLATE
Dosage Strength : 0.5MG
Packaging :
Approval Date : 1996-12-12
Application Number : 40103
Regulatory Info : RX
Registration Country : USA
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