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01 2Athena Pharmaceutiques

02 2Accel Pharma

03 5Accord healthcare

04 2Acme Lifetech

05 2Adcock Ingram

06 3American Regent

07 1Amneal Pharmaceuticals

08 7Apotex Inc

09 1Aristo Pharma GmbH

10 3Auro Pharma Inc

11 6Aurobindo Pharma Limited

12 2Avet Pharmaceuticals

13 3B. Braun Melsungen AG

14 2Baxter Healthcare Corporation

15 5Bexal Farmaceutica Sa

16 9Chartwell Pharmaceuticals llc

17 2EUGIA PHARMA INC.

18 1Eugia Pharma

19 2Farmalider SA

20 3Fresenius Kabi AB Brunna

21 3Fresenius Kabi USA

22 2GLAND PHARMA LIMITED

23 1GSK

24 3Glenmark Pharmaceuticals

25 3Glumex Pharmaceuticals Mfg. Pvt. Ltd

26 1Ha Noi CPC1 Pharmaceutical JSC

27 12Hikma Pharmaceuticals

28 6Hospira, Inc.

29 1Ind Swift Laboratories Limited

30 2Ipca Laboratories

31 2Ips Farma Sl

32 3JAMP PHARMA

33 1Kalcex

34 4LABORATORIOS NORMON SA

35 2Laboratorios Serra Pamies

36 1Lannett Company, Inc.

37 1Luitpold Pharmaceuticals, Inc.

38 3MARCAN PHARMACEUTICALS INC

39 3MINT PHARMACEUTICALS INC

40 2Medipol Pharmaceutical

41 2Myungmoon Pharm. Co., LTD.

42 2Natco Pharma

43 2Natco Pharma (Canada) Inc

44 4Neuraxpharm

45 1Nishchem International Pvt. Ltd

46 1Novartis Pharmaceuticals Corporation

47 2ONESOURCE SPECIALTY

48 1PHARM ASSOC

49 1PRO DOC LIMITEE

50 2Pharmascience Inc.

51 4Pliva Hrvatska

52 2Pluviaendo

53 1Polifarma

54 1Qilu Pharmaceutical

55 5Rising Pharmaceuticals Inc

56 2SANIS HEALTH INC

57 2SIVEM PHARMACEUTICALS ULC

58 2STERIMAX INC

59 1Sagent Pharmaceuticals

60 13Sandoz B2B

61 2Smith & Kenner Pharmaceuticals

62 10Sun Pharmaceutical Industries Limited

63 5Taro Pharmaceutical Industries

64 11Teva Pharmaceutical Industries

65 1Unicor Pharmatech

66 4Viatris

67 2Wockhardt

68 4XYZ Pharma

69 2Zydus Healthcare SA (Pty) Ltd

70 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

Luxepack
Not Confirmed
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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

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Not Confirmed
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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

Luxepack
Not Confirmed
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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

Luxepack
Not Confirmed
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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

Luxepack
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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

Luxepack
Not Confirmed
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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

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Not Confirmed
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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

Luxepack
Not Confirmed
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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

Luxepack
Not Confirmed
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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

Luxepack
Not Confirmed
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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

Luxepack
Not Confirmed
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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

Luxepack
Not Confirmed
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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

Luxepack
Not Confirmed
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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

Luxepack
Not Confirmed
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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

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XYZ Pharma

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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

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XYZ Pharma

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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

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XYZ Pharma

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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

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XYZ Pharma

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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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