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VKT Pharma
FDA Orange Book

Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.

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AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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xyz-pharma-m-2024-10-07

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EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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xyz-pharma-m-2024-10-07

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VKT Pharma

VISIT THE VIRTUAL BOOTH, Contact Details

VISIT THE VIRTUAL BOOTH
Review portfolio & marketing content
CONTACT DETAILS
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EVENTS

Webinars & Exhibitions

Webinars & Exhibitions

PRESENTATION(s)

Corporate Presentation

Corporate Presentation

DIGITAL CONTENT

INTERVIEW #SpeakPharma, VLOG #PharmaReel, DATA COMPILATION #PharmaFlow, 4 NEWS #PharmaBuzz

INTERVIEW #SpeakPharma
VLOG #PharmaReel
DATA COMPILATION #PharmaFlow
4 NEWS #PharmaBuzz

FINISHED DOSAGE FORMULATIONS

30 FDF Dossiers, 10 FDA Orange Book, 20 Listed Dossiers

30 FDF Dossiers
10 FDA Orange Book
20 Listed Dossiers

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FILTER :

filter Active Ingredients Reset all filters

10 All

01 2FAMOTIDINE

02 2RANITIDINE HYDROCHLORIDE

03 2RANOLAZINE

04 4TADALAFIL

filter Dosage Reset all filters

10 All

01 2TABLET, EXTENDED RELEASE;ORAL

02 8TABLET;ORAL

filter Dosage Strength Reset all filters

10 All

01 210MG

02 11GM

03 12.5MG

04 220MG

05 1500MG

06 15MG

07 1EQ 150MG BASE

08 1EQ 300MG BASE

filter Regulatory Info Reset all filters

10 All

01 2OTC

02 8RX

List of Suppliers

Supplier Virtual Booth

price-trend

01

Brand Name : FAMOTIDINE

2024 ACI Convention

Not Confirmed

Brand Name : FAMOTIDINE

2024 ACI Convention

Not Confirmed

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Digital Content

RLD : No

TE Code :

Dosage Form : TABLET; ORAL

Proprietary Name : FAMOTIDINE

Dosage Strength : 10MG

Approval Date : 2022-01-28

Application Number : 215822

RX/OTC/DISCN : OTC

RLD : No

TE Code :

Product
Web Link

Stock Recap
#PipelineProspector

02

Brand Name : FAMOTIDINE

2024 ACI Convention

Not Confirmed

Brand Name : FAMOTIDINE

2024 ACI Convention

Not Confirmed

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Digital Content

RLD : No

TE Code :

Dosage Form : TABLET; ORAL

Proprietary Name : FAMOTIDINE

Dosage Strength : 20MG

Approval Date : 2022-01-28

Application Number : 215822

RX/OTC/DISCN : OTC

RLD : No

TE Code :

Product
Web Link

Stock Recap
#PipelineProspector

03

Brand Name : RANITIDINE HYDROCHLO...

2024 ACI Convention

Not Confirmed

Brand Name : RANITIDINE HYDROCHLO...

2024 ACI Convention

Not Confirmed

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Digital Content

RLD : No

TE Code : AB

RANITIDINE HYDROCHLORIDE

Dosage Form : TABLET; ORAL

Proprietary Name : RANITIDINE HYDROCHLORIDE

Dosage Strength : EQ 150MG BASE

Approval Date : 2019-01-31

Application Number : 211289

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Product
Web Link

Stock Recap
#PipelineProspector

04

Brand Name : RANITIDINE HYDROCHLO...

2024 ACI Convention

Not Confirmed

Brand Name : RANITIDINE HYDROCHLO...

2024 ACI Convention

Not Confirmed

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Digital Content

RLD : No

TE Code : AB

RANITIDINE HYDROCHLORIDE

Dosage Form : TABLET; ORAL

Proprietary Name : RANITIDINE HYDROCHLORIDE

Dosage Strength : EQ 300MG BASE

Approval Date : 2019-01-31

Application Number : 211289

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Product
Web Link

Stock Recap
#PipelineProspector

05

Brand Name : RANOLAZINE

2024 ACI Convention

Not Confirmed

Brand Name : RANOLAZINE

2024 ACI Convention

Not Confirmed

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Digital Content

RLD : No

TE Code : AB

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Proprietary Name : RANOLAZINE

Dosage Strength : 500MG

Approval Date : 2022-01-19

Application Number : 214035

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Product
Web Link

Stock Recap
#PipelineProspector

06

Brand Name : RANOLAZINE

2024 ACI Convention

Not Confirmed

Brand Name : RANOLAZINE

2024 ACI Convention

Not Confirmed

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Digital Content

RLD : No

TE Code : AB

Dosage Form : TABLET, EXTENDED RELEASE; ORAL

Proprietary Name : RANOLAZINE

Dosage Strength : 1GM

Approval Date : 2022-01-19

Application Number : 214035

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Product
Web Link

Stock Recap
#PipelineProspector

07

Brand Name : TADALAFIL

2024 ACI Convention

Not Confirmed

Brand Name : TADALAFIL

2024 ACI Convention

Not Confirmed

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Digital Content

RLD : No

TE Code : AB1

Dosage Form : TABLET; ORAL

Proprietary Name : TADALAFIL

Dosage Strength : 2.5MG

Approval Date : 2021-11-04

Application Number : 215556

RX/OTC/DISCN : RX

RLD : No

TE Code : AB1

Product
Web Link

Stock Recap
#PipelineProspector

08

Brand Name : TADALAFIL

2024 ACI Convention

Not Confirmed

Brand Name : TADALAFIL

2024 ACI Convention

Not Confirmed

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Digital Content

RLD : No

TE Code : AB1

Dosage Form : TABLET; ORAL

Proprietary Name : TADALAFIL

Dosage Strength : 5MG

Approval Date : 2021-11-04

Application Number : 215556

RX/OTC/DISCN : RX

RLD : No

TE Code : AB1

Product
Web Link

Stock Recap
#PipelineProspector

09

Brand Name : TADALAFIL

2024 ACI Convention

Not Confirmed

Brand Name : TADALAFIL

2024 ACI Convention

Not Confirmed

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

Post an Enquiry

Post an Enquiry

Digital Content

RLD : No

TE Code : AB1

Dosage Form : TABLET; ORAL

Proprietary Name : TADALAFIL

Dosage Strength : 10MG

Approval Date : 2021-11-04

Application Number : 215556

RX/OTC/DISCN : RX

RLD : No

TE Code : AB1

Product
Web Link

Stock Recap
#PipelineProspector

10

Brand Name : TADALAFIL

2024 ACI Convention

Not Confirmed

Brand Name : TADALAFIL

2024 ACI Convention

Not Confirmed

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.

Post an Enquiry

Post an Enquiry

Digital Content

RLD : No

TE Code : AB1

Dosage Form : TABLET; ORAL

Proprietary Name : TADALAFIL

Dosage Strength : 20MG

Approval Date : 2021-11-04

Application Number : 215556

RX/OTC/DISCN : RX

RLD : No

TE Code : AB1

Product
Web Link

Stock Recap
#PipelineProspector

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