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23-26 March, 2026
BIO Partnering at JPMBIO Partnering at JPM
Industry Trade Show
Not Confirmed
12-15 January, 2026
Biotech ShowcaseBiotech Showcase
Industry Trade Show
Not Confirmed
12-14 January, 2026
Digital content

30 Oct 2025
// FDA

27 Jul 2025
// INDPHARMAPOST
https://www.indianpharmapost.com/drug-approval/concord-biotech-successfully-completes-russian-gmp-inspection-at-its-api-facility-17483

18 Jul 2025
// INDPHARMAPOST
https://www.indianpharmapost.com/news/concord-biotech-announces-successful-completion-eu-gmp-inspection-at-its-api-facility-17440

24 Jun 2025
// CAPTICALMRKT
https://www.capitalmarket.com/markets/news/live-news/concord-biotechs-api-facility-completes-usfda-inspection/1613344

03 May 2025
// INDPHARMAPOST
https://www.indianpharmapost.com/drug-approval/usfda-inspection-at-concord-biotechs-api-facility-at-dholka-17109

07 Apr 2025
// BUSINESS STD
https://www.business-standard.com/markets/capital-market-news/concord-biotech-gets-us-fda-nod-for-marketing-multiple-sclerosis-drug-teriflunomide-125040900207_1.html
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Details:
Teriflunomide is a pyrimidine synthesis inhibitor indicated for the treatment of relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease.
Lead Product(s): Teriflunomide,Inapplicable
Therapeutic Area: Neurology Brand Name: Teriflunomide-Generic
Study Phase: Approved FDFProduct Type: Miscellaneous
Sponsor: Undisclosed
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable April 07, 2025

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Lead Product(s) : Teriflunomide,Inapplicable
Therapeutic Area : Neurology
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Undisclosed
Deal Size : Inapplicable
Deal Type : Inapplicable
Concord Biotech gets US FDA Nod for Marketing Multiple Sclerosis Drug Teriflunomide
Details : Teriflunomide is a pyrimidine synthesis inhibitor indicated for the treatment of relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease.
Product Name : Teriflunomide-Generic
Product Type : Miscellaneous
Upfront Cash : Inapplicable
April 07, 2025

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Details:
Mycophenolate Mofetil Tablets are indicated for the prophylaxis of organ rejection in recipients of allogeneic kidney, heart or liver transplants, in combination with other immunosuppressants.
Lead Product(s): Mycophenolate Mofetil,Corticosteroids,Cyclosporine
Therapeutic Area: Immunology Brand Name: Mofecon
Study Phase: Approved FDFProduct Type: Antibiotic
Sponsor: Lupin Ltd
Deal Size: Inapplicable Upfront Cash: Inapplicable
Deal Type: Inapplicable August 06, 2020

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Lead Product(s) : Mycophenolate Mofetil,Corticosteroids,Cyclosporine
Therapeutic Area : Immunology
Highest Development Status : Approved FDF
Partner/Sponsor/Collaborator : Lupin Ltd
Deal Size : Inapplicable
Deal Type : Inapplicable
Lupin, Concord, Receive US FDA Approval for Mycophenolate Mofetil Tablets USP
Details : Mycophenolate Mofetil Tablets are indicated for the prophylaxis of organ rejection in recipients of allogeneic kidney, heart or liver transplants, in combination with other immunosuppressants.
Product Name : Mofecon
Product Type : Antibiotic
Upfront Cash : Inapplicable
August 06, 2020

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RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : MYCOPHENOLATE MOFETIL
Dosage Strength : 250MG
Approval Date : 2019-01-08
Application Number : 210181
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : MYCOPHENOLATE MOFETIL
Dosage Strength : 500MG
Approval Date : 2020-07-31
Application Number : 212087
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : MYCOPHENOLATE SODIUM
Dosage Strength : EQ 180MG BASE
Approval Date : 2019-12-13
Application Number : 211173
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : MYCOPHENOLATE SODIUM
Dosage Strength : EQ 360MG BASE
Approval Date : 2019-12-13
Application Number : 211173
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : TACROLIMUS
Dosage Strength : EQ 0.5MG BASE
Approval Date : 2020-11-10
Application Number : 213112
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : TACROLIMUS
Dosage Strength : EQ 1MG BASE
Approval Date : 2020-11-10
Application Number : 213112
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : CAPSULE; ORAL
Proprietary Name : TACROLIMUS
Dosage Strength : EQ 5MG BASE
Approval Date : 2020-11-10
Application Number : 213112
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : TERIFLUNOMIDE
Dosage Strength : 7MG
Approval Date : 2025-04-07
Application Number : 218663
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

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RLD : No
TE Code : AB
Dosage Form : TABLET; ORAL
Proprietary Name : TERIFLUNOMIDE
Dosage Strength : 14MG
Approval Date : 2025-04-07
Application Number : 218663
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

Services
API Manufacturing
Pharma Service : API Manufacturing
Category : Biologics, Bioprocess & Fermentation
Sub Category : Overview
Pharma Service : API Manufacturing
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Sales, Marketing, Registration
Inspections and registrations
Country : India
City/Region : Dholka Village
Audit Date : 2025-09-19
Audit Type : On-Site
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Concord Biotech is a supplier offers 55 products (APIs, Excipients or Intermediates).
Find a price of Cyclosporine bulk with DMF, CEP, JDMF, WC offered by Concord Biotech
Find a price of Mycophenolate Mofetil bulk with DMF, CEP, JDMF, WC offered by Concord Biotech
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