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NEWS #PharmaBuzz
01 Dec 2025
// PR NEWSWIRE
https://www.prnewswire.com/news-releases/biocodex-to-present-new-data-at-the-american-epilepsy-society-aes-2025-annual-meeting-302620684.html
04 Sep 2025
// PHARMAWEB
https://www.pharmiweb.com/press-release/2025-09-04/biocodex-invests-up-to-30-million-in-mrm-health-a-belgian-microbiome-therapy-innovator
04 Sep 2025
// PHARMAWEB
https://www.pharmiweb.com/press-release/2025-09-04/mrm-health-raises-55-million-series-b-to-advance-best-in-class-microbiome-based-biotherapeutic-prod
02 Sep 2025
// GLOBENEWSWIRE
https://www.globenewswire.com/news-release/2025/09/02/3142576/0/en/REMINDER-Biocodex-Microbiota-Foundation-invites-Canadian-academics-and-scientists-to-apply-for-35-000-research-grant.html
16 Jun 2025
// GLOBENEWSWIRE
https://www.globenewswire.com/news-release/2025/06/16/3100172/0/en/Biocodex-Microbiota-Foundation-invites-Canadian-academics-and-scientists-to-apply-for-35-000-research-grant.html
16 Dec 2024
// BUSINESSWIRE
Drugs in Development
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDA Orange Book
Dosage Form : CAPSULE; ORAL
Proprietary Name : DIACOMIT
Dosage Strength : 250MG
Approval Date : 2018-08-20
Application Number : 206709
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
Dosage Form : CAPSULE; ORAL
Proprietary Name : DIACOMIT
Dosage Strength : 500MG
Approval Date : 2018-08-20
Application Number : 206709
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : DIACOMIT
Dosage Strength : 250MG/PACKET
Approval Date : 2018-08-20
Application Number : 207223
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
Dosage Form : FOR SUSPENSION; ORAL
Proprietary Name : DIACOMIT
Dosage Strength : 500MG/PACKET
Approval Date : 2018-08-20
Application Number : 207223
RX/OTC/DISCN : RX
RLD : Yes
TE Code :
Europe
Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Oral Solution
Dosage Strength : 1G
Packaging :
Brand Name : Stimol
Approval Date : 2000-03-15
Application Number : 62951
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Oral Solution
Dosage Strength : 100ML
Packaging :
Brand Name : Stimol
Approval Date : 2006-02-28
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
Regulatory Info : Withdrawn
Registration Country : Malta
Dosage Form : Effervescent Powder
Dosage Strength : 1G
Packaging :
Brand Name : Stimol
Approval Date : 2010-08-17
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta
Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Hard Capsule
Dosage Strength : 0.05G
Packaging :
Brand Name : Stresam
Approval Date : 2006-02-28
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
Regulatory Info : Authorised
Registration Country : Malta
Lidocaine Hydrochloride; Phenazone
Dosage Form : Ear Drop Solution
Dosage Strength : 1%W/W; 4%W/W
Packaging :
Brand Name : Otipax Ear
Approval Date : 2006-02-28
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
Regulatory Info : Withdrawn
Registration Country : Malta
Dosage Form : Solution For Injection
Dosage Strength : 10MG/ML
Packaging :
Brand Name : Acupan
Approval Date : 2010-02-22
Application Number :
Regulatory Info : Withdrawn
Registration Country : Malta
Regulatory Info : Cancelled
Registration Country : Spain
Dosage Form : Hard Capsule
Dosage Strength : 50MG
Packaging :
Brand Name : Ultra Yeast
Approval Date : 2016-09-22
Application Number : 34009325988541
Regulatory Info : Cancelled
Registration Country : Spain
Regulatory Info : Authorized
Registration Country : Spain
Dosage Form : Capsule
Dosage Strength :
Packaging :
Brand Name : Ultra Yeast Capsules
Approval Date : 2004-05-28
Application Number : 311001-9
Regulatory Info : Authorized
Registration Country : Spain
Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Powder For Oral Solution
Dosage Strength : 250MG
Packaging :
Brand Name : Bioflor Powder For Oral
Approval Date : 2006-02-27
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
Regulatory Info : Authorised
Registration Country : Malta
Dosage Form : Capsule
Dosage Strength : 250MG
Packaging :
Brand Name : Bioflor
Approval Date : 2006-02-27
Application Number :
Regulatory Info : Authorised
Registration Country : Malta
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]ABOUT THIS PAGE
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