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01 2Athena Pharmaceutiques

02 2Accel Pharma

03 2Accord healthcare

04 2Acme Lifetech

05 2Adcock Ingram

06 3American Regent

07 1Amneal Pharmaceuticals

08 7Apotex Inc

09 3Auro Pharma Inc

10 6Aurobindo Pharma Limited

11 2Avet Pharmaceuticals

12 2Baxter Healthcare Corporation

13 9Chartwell Pharmaceuticals llc

14 2EUGIA PHARMA INC.

15 3Fresenius Kabi USA

16 2GLAND PHARMA LIMITED

17 1GSK

18 3Glenmark Pharmaceuticals

19 3Glumex Pharmaceuticals Mfg. Pvt. Ltd

20 1Ha Noi CPC1 Pharmaceutical JSC

21 10Hikma Pharmaceuticals

22 6Hospira, Inc.

23 1Ind Swift Laboratories Limited

24 2Ipca Laboratories

25 3JAMP PHARMA

26 1Lannett Company, Inc.

27 1Luitpold Pharmaceuticals, Inc.

28 3MARCAN PHARMACEUTICALS INC

29 3MINT PHARMACEUTICALS INC

30 2Medipol Pharmaceutical

31 2Myungmoon Pharm. Co., LTD.

32 2Natco Pharma

33 2Natco Pharma (Canada) Inc

34 1Nishchem International Pvt. Ltd

35 2ONESOURCE SPECIALTY

36 1PHARM ASSOC

37 1PRO DOC LIMITEE

38 2Pharmascience Inc.

39 4Pliva Hrvatska

40 2Pluviaendo

41 1Polifarma

42 1Qilu Pharmaceutical

43 5Rising Pharmaceuticals Inc

44 2SANIS HEALTH INC

45 2SIVEM PHARMACEUTICALS ULC

46 2STERIMAX INC

47 1Sagent Pharmaceuticals

48 13Sandoz B2B

49 2Smith & Kenner Pharmaceuticals

50 10Sun Pharmaceutical Industries Limited

51 5Taro Pharmaceutical Industries

52 7Teva Pharmaceutical Industries

53 1Unicor Pharmatech

54 2Viatris

55 2Wockhardt

56 4XYZ Pharma

57 1Blank

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAthena Pharmaceutiques is a Partner of Choice for Drug Delivery & Life Cycle Management.

Regulatory Info :

Registration Country : France

Ondansetron Hydrochloride

Brand Name : Ondansetron HCl

Dosage Form : Oro-Dispersible Tablet

Dosage Strength : 4MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : France

Athena Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAthena Pharmaceutiques is a Partner of Choice for Drug Delivery & Life Cycle Management.

Regulatory Info :

Registration Country : France

Ondansetron Hydrochloride

Brand Name : Ondansetron Hydrochloride

Dosage Form : Oro-Dispersible Tablet

Dosage Strength : 8MG

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : France

Athena Company Banner

03

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ZOFRAN AND DEXTROSE IN PLASTIC CONTAINER

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 0.64MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1995-01-31

Application Number : 20403

Regulatory Info : DISCN

Registration Country : USA

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04

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ONDANSETRON HYDROCHLORIDE PRESERVATIVE FREE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2MG BASE/ML

Packaging :

Approval Date : 2006-12-26

Application Number : 76780

Regulatory Info : DISCN

Registration Country : USA

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05

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ONDANSETRON HYDROCHLORIDE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2MG BASE/ML

Packaging :

Approval Date : 2006-12-26

Application Number : 76695

Regulatory Info : DISCN

Registration Country : USA

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06

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ONDANSETRON HYDROCHLORIDE PRESERVATIVE FREE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2MG BASE/ML

Packaging :

Approval Date : 2006-12-26

Application Number : 76696

Regulatory Info : DISCN

Registration Country : USA

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07

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ZOFRAN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1991-01-04

Application Number : 20007

Regulatory Info : DISCN

Registration Country : USA

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08

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ZOFRAN PRESERVATIVE FREE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1993-12-10

Application Number : 20007

Regulatory Info : DISCN

Registration Country : USA

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09

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ZOFRAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1992-12-31

Application Number : 20103

Regulatory Info : DISCN

Registration Country : USA

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10

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ZOFRAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 8MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1992-12-31

Application Number : 20103

Regulatory Info : DISCN

Registration Country : USA

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11

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ZOFRAN

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 24MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1999-08-27

Application Number : 20103

Regulatory Info : DISCN

Registration Country : USA

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12

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ZOFRAN

Dosage Form : SOLUTION;ORAL

Dosage Strength : EQ 4MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1997-01-24

Application Number : 20605

Regulatory Info : DISCN

Registration Country : USA

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13

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ONDANSETRON HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 4MG BASE

Packaging :

Approval Date : 2007-06-25

Application Number : 76252

Regulatory Info : DISCN

Registration Country : USA

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14

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ONDANSETRON HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 8MG BASE

Packaging :

Approval Date : 2007-06-25

Application Number : 76252

Regulatory Info : DISCN

Registration Country : USA

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15

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ONDANSETRON HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 24MG BASE

Packaging :

Approval Date : 2007-06-25

Application Number : 76252

Regulatory Info : DISCN

Registration Country : USA

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16

Pharmex
Not Confirmed
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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ONDANSETRON HYDROCHLORIDE PRESERVATIVE FREE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : EQ 2MG BASE/ML

Packaging :

Approval Date : 2006-11-22

Application Number : 76759

Regulatory Info : DISCN

Registration Country : USA

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17

XYZ Pharma

Pharmex
Not Confirmed
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XYZ Pharma

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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ONDANSETRON HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 24MG BASE

Packaging :

Approval Date : 2006-12-26

Application Number : 76183

Regulatory Info : DISCN

Registration Country : USA

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18

XYZ Pharma

Pharmex
Not Confirmed
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XYZ Pharma

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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ONDANSETRON HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 8MG BASE

Packaging :

Approval Date : 2006-12-26

Application Number : 76183

Regulatory Info : RX

Registration Country : USA

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19

XYZ Pharma

Pharmex
Not Confirmed
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XYZ Pharma

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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ONDANSETRON HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 4MG BASE

Packaging :

Approval Date : 2006-12-26

Application Number : 76183

Regulatory Info : RX

Registration Country : USA

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20

XYZ Pharma

Pharmex
Not Confirmed
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XYZ Pharma

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Pharmex
Not Confirmed

ONDANSETRON HYDROCHLORIDE

Brand Name : ONDANSETRON HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 16MG BASE

Packaging :

Approval Date : 2006-12-26

Application Number : 76183

Regulatory Info : DISCN

Registration Country : USA

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