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01 6Towa Pharmaceutical

02 1Accord healthcare

03 1Altan Pharma

04 2Alter Laboratories Sa

05 2AstraZeneca

06 2Aurobindo Pharma Limited

07 2Aurovitas Spain, Sau

08 2Bio Labs

09 4Cinfa

10 1Demo S.A.

11 2Deva Holding AS

12 1Epic Pharma. LLC.

13 2GLAND PHARMA LIMITED

14 2Hainan Poly Pharm

15 2Kern Pharma S.L.

16 3LABORATORIOS NORMON SA

17 1Leeford Healthcare

18 2Mabo Farma

19 1Naprod Life Sciences

20 2PHARMOBEDIENT

21 1Polifarma

22 1Rajasthan Antibiotics

23 2Reyoung pharmaceutical

24 1Sandoz B2B

25 1Senov Life Science

26 1Slate Run Pharmaceuticals

27 1Stanex Drugs and Chemicals

28 2Sun Pharmaceutical Industries Limited

29 2Teva Pharmaceutical Industries

30 1Yangtze River Pharmaceutical Group

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTowa Pharma is dedicated to researching, developing, producing, and promoting generic drugs.

Regulatory Info : Authorized

Registration Country : Spain

Esomeprazole Sodium

Brand Name : Esomeprazol Pensa

Dosage Form : Gastro-Resistant Hard Capsule

Dosage Strength : 40MG

Packaging :

Approval Date : 2018-02-08

Application Number : 82848

Regulatory Info : Authorized

Registration Country : Spain

Towa Pharmaceutical

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTowa Pharma is dedicated to researching, developing, producing, and promoting generic drugs.

Regulatory Info : Authorized

Registration Country : Spain

Esomeprazole Sodium

Brand Name : Esomeprazol Pensa

Dosage Form : Gastro-Resistant Tablet

Dosage Strength : 40MG

Packaging :

Approval Date : 2011-11-23

Application Number : 75076

Regulatory Info : Authorized

Registration Country : Spain

Towa Pharmaceutical

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTowa Pharma is dedicated to researching, developing, producing, and promoting generic drugs.

Regulatory Info : Authorized

Registration Country : Spain

Esomeprazole Sodium

Brand Name : Esomeprazol Pensa

Dosage Form : Gastro-Resistant Hard Capsule

Dosage Strength : 20MG

Packaging :

Approval Date : 2018-02-08

Application Number : 82847

Regulatory Info : Authorized

Registration Country : Spain

Towa Pharmaceutical

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTowa Pharma is dedicated to researching, developing, producing, and promoting generic drugs.

Regulatory Info : Suspensed

Registration Country : Spain

Esomeprazole Sodium

Brand Name : Noecel

Dosage Form : Gastro-Resistant Tablet

Dosage Strength : 20MG

Packaging :

Approval Date : 2011-11-23

Application Number : 75058

Regulatory Info : Suspensed

Registration Country : Spain

Towa Pharmaceutical

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTowa Pharma is dedicated to researching, developing, producing, and promoting generic drugs.

Regulatory Info : Suspensed

Registration Country : Spain

Esomeprazole Sodium

Brand Name : Noecel

Dosage Form : Gastro-Resistant Tablet

Dosage Strength : 40MG

Packaging :

Approval Date : 2011-11-23

Application Number : 75060

Regulatory Info : Suspensed

Registration Country : Spain

Towa Pharmaceutical

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTowa Pharma is dedicated to researching, developing, producing, and promoting generic drugs.

Regulatory Info : Authorized

Registration Country : Spain

Esomeprazole Sodium

Brand Name : Esomeprazol Pensa

Dosage Form : Gastro-Resistant Tablet

Dosage Strength : 20MG

Packaging :

Approval Date : 2011-11-23

Application Number : 75075

Regulatory Info : Authorized

Registration Country : Spain

Towa Pharmaceutical

07

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ESOMEPRAZOLE SODIUM

Brand Name : ESOMEPRAZOLE SODIUM

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 40MG BASE/VIAL

Packaging :

Approval Date : 2015-09-25

Application Number : 205379

Regulatory Info : DISCN

Registration Country : USA

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08

The MedTech Conference
Not Confirmed
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The MedTech Conference
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ESOMEPRAZOLE SODIUM

Brand Name : NEXIUM IV

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 20MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 2005-03-31

Application Number : 21689

Regulatory Info : DISCN

Registration Country : USA

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09

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ESOMEPRAZOLE SODIUM

Brand Name : NEXIUM IV

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 40MG BASE/VIAL

Packaging :

Approval Date : 2005-03-31

Application Number : 21689

Regulatory Info : DISCN

Registration Country : USA

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10

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ESOMEPRAZOLE SODIUM

Brand Name : ESOMEPRAZOLE SODIUM

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 20MG BASE/VIAL

Packaging :

Approval Date : 2016-08-10

Application Number : 204657

Regulatory Info : DISCN

Registration Country : USA

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11

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ESOMEPRAZOLE SODIUM

Brand Name : ESOMEPRAZOLE SODIUM

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 40MG BASE/VIAL

Packaging :

Approval Date : 2016-08-10

Application Number : 204657

Regulatory Info : DISCN

Registration Country : USA

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12

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ESOMEPRAZOLE SODIUM

Brand Name : ESOMEPRAZOLE SODIUM

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 40MG BASE/VIAL

Packaging :

Approval Date : 2017-03-06

Application Number : 207181

Regulatory Info : RX

Registration Country : USA

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13

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ESOMEPRAZOLE SODIUM

Brand Name : ESOMEPRAZOLE SODIUM

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 40MG BASE/VIAL

Packaging :

Approval Date : 2025-01-08

Application Number : 214046

Regulatory Info : RX

Registration Country : USA

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14

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ESOMEPRAZOLE SODIUM

Brand Name : ESOMEPRAZOLE SODIUM

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 20MG BASE/VIAL

Packaging :

Approval Date : 2020-04-01

Application Number : 203349

Regulatory Info : RX

Registration Country : USA

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15

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ESOMEPRAZOLE SODIUM

Brand Name : ESOMEPRAZOLE SODIUM

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 40MG BASE/VIAL

Packaging :

Approval Date : 2020-04-01

Application Number : 203349

Regulatory Info : RX

Registration Country : USA

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16

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ESOMEPRAZOLE SODIUM

Brand Name : ESOMEPRAZOLE SODIUM

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 40MG BASE/VIAL

Packaging :

Approval Date : 2022-02-10

Application Number : 215732

Regulatory Info : RX

Registration Country : USA

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17

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ESOMEPRAZOLE SODIUM

Brand Name : ESOMEPRAZOLE SODIUM

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 20MG BASE/VIAL

Packaging :

Approval Date : 2013-03-18

Application Number : 200882

Regulatory Info : DISCN

Registration Country : USA

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18

The MedTech Conference
Not Confirmed
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The MedTech Conference
Not Confirmed

ESOMEPRAZOLE SODIUM

Brand Name : ESOMEPRAZOLE SODIUM

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 40MG BASE/VIAL

Packaging :

Approval Date : 2013-03-18

Application Number : 200882

Regulatory Info : DISCN

Registration Country : USA

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19

PHARMOBEDIENT

Country
The MedTech Conference
Not Confirmed
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PHARMOBEDIENT

Country
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The MedTech Conference
Not Confirmed

ESOMEPRAZOLE SODIUM

Brand Name : ESOMEPRAZOLE SODIUM

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 20MG BASE/VIAL

Packaging :

Approval Date : 2017-05-17

Application Number : 202686

Regulatory Info : DISCN

Registration Country : USA

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20

PHARMOBEDIENT

Country
The MedTech Conference
Not Confirmed
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PHARMOBEDIENT

Country
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The MedTech Conference
Not Confirmed

ESOMEPRAZOLE SODIUM

Brand Name : ESOMEPRAZOLE SODIUM

Dosage Form : INJECTABLE;INTRAVENOUS

Dosage Strength : EQ 40MG BASE/VIAL

Packaging :

Approval Date : 2017-05-17

Application Number : 202686

Regulatory Info : DISCN

Registration Country : USA

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