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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 1ASPIRO

09 3AUROBINDO PHARMA LTD

10 3BAXTER HLTHCARE CORP

11 1BE PHARMS

12 1CIPLA

13 1DEXCEL

14 2DR REDDYS LABS LTD

15 1EPIC PHARMA LLC

16 1EUGIA PHARMA

17 1FRESENIUS KABI USA

18 1GLAND

19 2GRAVITI PHARMS

20 1HANGZHOU ZHONGMEI

21 2HETERO LABS LTD V

22 1HIKMA

23 1INGENUS PHARMS LLC

24 2JUBILANT GENERICS

25 1KNACK

26 1L PERRIGO CO

27 2LANNETT CO INC

28 2MACLEODS PHARMS LTD

29 1MEITHEAL

30 2MYLAN PHARMS INC

31 1NORVIUM BIOSCIENCE

32 2ORBION PHARMS

33 2RUBICON

34 1SANDOZ

35 4SUN PHARM

36 2SUN PHARM INDS LTD

37 2TEVA

38 1TEVA PARENTERAL

39 2TORRENT PHARMS

40 2WOCKHARDT BIO AG

41 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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
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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