27 Oct 2025
// FDA
05 Aug 2025
// EXPRESSPHARMA
01 Aug 2025
// PR NEWSWIRE
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Industry Trade Show
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23-26 March, 2026
Industry Trade Show
Attending
21-23 April, 2026
Industry Trade Show
Exhibiting
16-18 May, 2026

27 Oct 2025
// FDA
https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=218205

05 Aug 2025
// EXPRESSPHARMA
https://www.expresspharma.in/zenara-pharma-receives-us-fda-approval-for-generic-sertraline-hydrochloride-capsules/

01 Aug 2025
// PR NEWSWIRE
https://www.prnewswire.com/news-releases/zenara-pharma-receives-us-fda-approval--for-first-generic-of-sertraline-hydrochloride-capsules-with-180-day-cgt-exclusivity-302519297.html

16 Jul 2025
// FDA
https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&varApplNo=218853

11 Jun 2025
// FDA
https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=218797

03 Feb 2025
// FDA
https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=214844
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Details:
Sertraline HCl, a miscellaneous product targeting SSR, shows promising results in treating undisclosed Key Focus Area.
Lead Product(s): Sertraline Hydrochloride
Therapeutic Area: Psychiatry/Psychology Brand Name: Sertraline-HCl
Study Phase: Approved FDFProduct Type: Miscellaneous
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable August 01, 2025
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Lead Product(s) : Sertraline Hydrochloride
Therapeutic Area : Psychiatry/Psychology
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Details : Sertraline HCl, a miscellaneous product targeting SSR, shows promising results in treating undisclosed Key Focus Area.
Product Name : Sertraline-HCl
Product Type : Miscellaneous
Upfront Cash : Inapplicable
August 01, 2025
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Details:
Cannabinoid oral solution has received approval for the treatment of several neurological disorders. It functions by stimulating two receptors, cannabinoid receptor type 1 and type 2, within the endocannabinoid system, maintaining body's homeostatis.
Lead Product(s): Cannabidiol
Therapeutic Area: Rare Diseases and Disorders Brand Name: Undisclosed
Study Phase: Approved FDFProduct Type: Controlled Substance
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable May 15, 2023
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Lead Product(s) : Cannabidiol
Therapeutic Area : Rare Diseases and Disorders
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Biophore, Its Subsidiary Zenara Pharma, Receive First Approval for Cannabidiol in India
Details : Cannabinoid oral solution has received approval for the treatment of several neurological disorders. It functions by stimulating two receptors, cannabinoid receptor type 1 and type 2, within the endocannabinoid system, maintaining body's homeostatis.
Product Name : Undisclosed
Product Type : Controlled Substance
Upfront Cash : Inapplicable
May 15, 2023
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Paxzen (nirmatrelvir) is an oral protease inhibitor that is active against MPRO, a viral protease that plays an essential role in viral replication by cleaving the 2 viral polyproteins.
Lead Product(s): Nirmatrelvir,Ritonavir
Therapeutic Area: Infections and Infectious Diseases Brand Name: Paxzen
Study Phase: Approved FDFProduct Type: Miscellaneous
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable September 09, 2022
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Lead Product(s) : Nirmatrelvir,Ritonavir
Therapeutic Area : Infections and Infectious Diseases
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Zenara Launches Generic Version Of Pfizer Covid Drug Paxlovid
Details : Paxzen (nirmatrelvir) is an oral protease inhibitor that is active against MPRO, a viral protease that plays an essential role in viral replication by cleaving the 2 viral polyproteins.
Product Name : Paxzen
Product Type : Miscellaneous
Upfront Cash : Inapplicable
September 09, 2022
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Zenara said Nirmatrelvir and Ritonavir tablets will soon be available in a combi-pack, sold under the brand name Paxzen, as a treatment of mild-to-moderate Covid-19 in adults.
Lead Product(s): Nirmatrelvir,Ritonavir
Therapeutic Area: Infections and Infectious Diseases Brand Name: Paxzen
Study Phase: Approved FDFProduct Type: Miscellaneous
Sponsor: Pfizer Inc
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable July 28, 2022
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Lead Product(s) : Nirmatrelvir,Ritonavir
Therapeutic Area : Infections and Infectious Diseases
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Pfizer Inc
Deal Size : Inapplicable
Deal Type : Inapplicable
Zenara Pharma to Launch Generic Paxlovid Soon
Details : Zenara said Nirmatrelvir and Ritonavir tablets will soon be available in a combi-pack, sold under the brand name Paxzen, as a treatment of mild-to-moderate Covid-19 in adults.
Product Name : Paxzen
Product Type : Miscellaneous
Upfront Cash : Inapplicable
July 28, 2022
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Favipiravir tablets will be sold under the brand name ‘Favizen’, is being manufactured at Zenara’s US FDA approved facility in Hyderabad.
Lead Product(s): Favipiravir
Therapeutic Area: Infections and Infectious Diseases Brand Name: Favizen
Study Phase: Approved FDFProduct Type: Miscellaneous
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable August 05, 2020
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Lead Product(s) : Favipiravir
Therapeutic Area : Infections and Infectious Diseases
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Zenara Pharma, a Biophore Subsidiary, Gets DCGI Nod for Favipiravir Tablets
Details : Favipiravir tablets will be sold under the brand name ‘Favizen’, is being manufactured at Zenara’s US FDA approved facility in Hyderabad.
Product Name : Favizen
Product Type : Miscellaneous
Upfront Cash : Inapplicable
August 05, 2020
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Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BREXPIPRAZOLE
Dosage Strength : 0.25MG
Packaging :
Approval Date :
Application Number : 213477
Regulatory Info :
Registration Country : USA
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Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BREXPIPRAZOLE
Dosage Strength : 0.5MG
Packaging :
Approval Date :
Application Number : 213477
Regulatory Info :
Registration Country : USA
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Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BREXPIPRAZOLE
Dosage Strength : 1MG
Packaging :
Approval Date :
Application Number : 213477
Regulatory Info :
Registration Country : USA
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Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BREXPIPRAZOLE
Dosage Strength : 2MG
Packaging :
Approval Date :
Application Number : 213477
Regulatory Info :
Registration Country : USA
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Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BREXPIPRAZOLE
Dosage Strength : 3MG
Packaging :
Approval Date :
Application Number : 213477
Regulatory Info :
Registration Country : USA
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Regulatory Info :
Registration Country : USA
Dosage Form : TABLET;ORAL
Brand Name : BREXPIPRAZOLE
Dosage Strength : 4MG
Packaging :
Approval Date :
Application Number : 213477
Regulatory Info :
Registration Country : USA
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Regulatory Info :
Registration Country : USA
Dosage Form : TABLET
Brand Name : CENOBAMATE
Dosage Strength : 50MG
Packaging :
Approval Date :
Application Number : 219403
Regulatory Info :
Registration Country : USA
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Regulatory Info :
Registration Country : USA
Dosage Form : TABLET
Brand Name : CENOBAMATE
Dosage Strength : 200MG
Packaging :
Approval Date :
Application Number : 219403
Regulatory Info :
Registration Country : USA
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Regulatory Info :
Registration Country : USA
Dosage Form : TABLET
Brand Name : CENOBAMATE
Dosage Strength : 100MG
Packaging :
Approval Date :
Application Number : 219403
Regulatory Info :
Registration Country : USA
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Regulatory Info :
Registration Country : USA
Dosage Form : TABLET
Brand Name : CENOBAMATE
Dosage Strength : 25MG
Packaging :
Approval Date :
Application Number : 219403
Regulatory Info :
Registration Country : USA
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RLD :
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BREXPIPRAZOLE
Dosage Strength : 0.25MG
Approval Date :
Application Number : 213477
RX/OTC/DISCN :
RLD :
TE Code :
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RLD :
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BREXPIPRAZOLE
Dosage Strength : 0.5MG
Approval Date :
Application Number : 213477
RX/OTC/DISCN :
RLD :
TE Code :
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RLD :
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BREXPIPRAZOLE
Dosage Strength : 1MG
Approval Date :
Application Number : 213477
RX/OTC/DISCN :
RLD :
TE Code :
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RLD :
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BREXPIPRAZOLE
Dosage Strength : 2MG
Approval Date :
Application Number : 213477
RX/OTC/DISCN :
RLD :
TE Code :
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RLD :
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BREXPIPRAZOLE
Dosage Strength : 3MG
Approval Date :
Application Number : 213477
RX/OTC/DISCN :
RLD :
TE Code :
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RLD :
TE Code :
Dosage Form : TABLET; ORAL
Proprietary Name : BREXPIPRAZOLE
Dosage Strength : 4MG
Approval Date :
Application Number : 213477
RX/OTC/DISCN :
RLD :
TE Code :
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RLD :
TE Code :
Dosage Form : TABLET
Proprietary Name : CENOBAMATE
Dosage Strength : 50MG
Approval Date :
Application Number : 219403
RX/OTC/DISCN :
RLD :
TE Code :
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RLD :
TE Code :
Dosage Form : TABLET
Proprietary Name : CENOBAMATE
Dosage Strength : 200MG
Approval Date :
Application Number : 219403
RX/OTC/DISCN :
RLD :
TE Code :
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RLD :
TE Code :
Dosage Form : TABLET
Proprietary Name : CENOBAMATE
Dosage Strength : 100MG
Approval Date :
Application Number : 219403
RX/OTC/DISCN :
RLD :
TE Code :
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RLD :
TE Code :
Dosage Form : TABLET
Proprietary Name : CENOBAMATE
Dosage Strength : 25MG
Approval Date :
Application Number : 219403
RX/OTC/DISCN :
RLD :
TE Code :
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