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01 2GRANULES

02 2MANKIND PHARMA

03 2ACTAVIS TOTOWA

04 1AJANTA PHARMA LTD

05 1ALEMBIC

06 2AMNEAL PHARMS

07 1ANNORA PHARMA

08 2APOTEX

09 1ASPIRO

10 3AUROBINDO PHARMA LTD

11 3BAXTER HLTHCARE CORP

12 1BE PHARMS

13 1CIPLA

14 1DEVA HOLDING AS

15 1DEXCEL

16 2DR REDDYS LABS LTD

17 1EPIC PHARMA LLC

18 1EUGIA PHARMA

19 1FRESENIUS KABI USA

20 1GLAND

21 2GRAVITI PHARMS

22 1HANGZHOU ZHONGMEI

23 2HETERO LABS LTD V

24 1HIKMA

25 1INGENUS PHARMS LLC

26 2JUBILANT GENERICS

27 1KNACK

28 1L PERRIGO CO

29 2LANNETT CO INC

30 2MACLEODS PHARMS LTD

31 1MEITHEAL

32 2MYLAN PHARMS INC

33 1NORVIUM BIOSCIENCE

34 2ORBION PHARMS

35 2RUBICON RESEARCH

36 1SANDOZ

37 4SUN PHARM

38 2SUN PHARM INDS LTD

39 2TEVA

40 1TEVA PARENTERAL

41 2TORRENT PHARMS

42 4WYETH PHARMS

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothGranules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

RLD : No

TE Code : AB

PANTOPRAZOLE SODIUM

Brand Name : PANTOPRAZOLE SODIUM

Dosage Form : TABLET, DELAYED RELEASE;ORAL

Dosage Strength : EQ 20MG BASE

Approval Date : 2023-12-11

Application Number : 217282

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Granules India

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

RLD : No

TE Code : AB

PANTOPRAZOLE SODIUM

Brand Name : PANTOPRAZOLE SODIUM

Dosage Form : TABLET, DELAYED RELEASE;ORAL

Dosage Strength : EQ 40MG BASE

Approval Date : 2022-07-26

Application Number : 215880

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothGranules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

RLD : No

TE Code : AB

PANTOPRAZOLE SODIUM

Brand Name : PANTOPRAZOLE SODIUM

Dosage Form : TABLET, DELAYED RELEASE;ORAL

Dosage Strength : EQ 40MG BASE

Approval Date : 2023-12-11

Application Number : 217282

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

Granules India

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDelivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.

RLD : No

TE Code :

PANTOPRAZOLE SODIUM

Brand Name : PANTOPRAZOLE SODIUM

Dosage Form : TABLET, DELAYED RELEASE;ORAL

Dosage Strength : EQ 20MG BASE

Approval Date : 2024-04-25

Application Number : 215880

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

Company Banner

05

ISPOR Europe 2025
Not Confirmed
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ISPOR Europe 2025
Not Confirmed

PANTOPRAZOLE SODIUM

Brand Name : PANTOPRAZOLE SODIUM

Dosage Form : INJECTABLE; INJECTION

Dosage Strength : 40MG

Approval Date :

Application Number : 22226

RX/OTC/DISCN :

RLD :

TE Code :

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06

ISPOR Europe 2025
Not Confirmed
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ISPOR Europe 2025
Not Confirmed

PANTOPRAZOLE SODIUM

Brand Name : PANTOPRAZOLE SODIUM

Dosage Form : TABLET, DELAYED RELEASE;ORAL

Dosage Strength : EQ 20MG BASE

Approval Date : 2007-08-02

Application Number : 77056

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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07

ISPOR Europe 2025
Not Confirmed
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ISPOR Europe 2025
Not Confirmed

PANTOPRAZOLE SODIUM

Brand Name : PROTONIX

Dosage Form : TABLET, DELAYED RELEASE;ORAL

Dosage Strength : EQ 40MG BASE

Approval Date : 2000-02-02

Application Number : 20987

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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08

ISPOR Europe 2025
Not Confirmed
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ISPOR Europe 2025
Not Confirmed

PANTOPRAZOLE SODIUM

Brand Name : PROTONIX

Dosage Form : TABLET, DELAYED RELEASE;ORAL

Dosage Strength : EQ 20MG BASE

Approval Date : 2001-06-12

Application Number : 20987

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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09

ISPOR Europe 2025
Not Confirmed
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ISPOR Europe 2025
Not Confirmed

PANTOPRAZOLE SODIUM

Brand Name : PROTONIX IV

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 40MG BASE/VIAL

Approval Date : 2001-03-22

Application Number : 20988

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AP

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10

ISPOR Europe 2025
Not Confirmed
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ISPOR Europe 2025
Not Confirmed

PANTOPRAZOLE SODIUM

Brand Name : PROTONIX

Dosage Form : FOR SUSPENSION, DELAYED RELEASE;ORAL

Dosage Strength : EQ 40MG BASE

Approval Date : 2007-11-14

Application Number : 22020

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

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