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

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01 2Ampoule
02 4DSP
03 2FCT
04 28Film Coated Tablet
05 4INJ
06 51INJECTABLE;INJECTION
07 3INJECTION
08 1Injectable And Infusion Solution
09 2Injectable And Infusion Solution In Pre-Filled Syringe
10 1Injectable And Perfusion Solution
11 17Injectable Solution
12 2Injection
13 1Injection / Infusion Solution
14 2ORALLY DISINTEGRATING TABLET
15 2Oral Lyophilized
16 1Oral Solution
17 2Oro-Dispersible Tablet
18 14SOLUTION
19 7SOLUTION;ORAL
20 10Solution For Injection
21 1Solution For Injection And Infusion
22 6Solution For Injection/Infusion
23 4Solution For Perfusion
24 7Syrup
25 2TAB
26 25TABLET
27 2TABLET; ORAL
28 42TABLET;ORAL
29 5Tablet
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01 1Authorised
02 33Authorized
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04 65DISCN
05 15Generic
06 29Marketed
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08 39Prescription
09 35RX
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01 2ACCEL-ONDANSETRON
02 3APO-ONDANSETRON
03 2AURO-ONDANSETRON INJECTION
04 2EUGIA-ONDANSETRON INJECTION
05 1JAMP ONDANSETRON
06 2JAMP-ONDANSETRON
07 2MAR-ONDANSETRON
08 2MINT-ONDANSETRON
09 1MINT-ONDANSETRON SOLUTION
10 2MYLAN-ONDANSETRON
11 2NAT-ONDANSETRON
12 1Nausazy
13 5ONDANSETRON
14 74ONDANSETRON HYDROCHLORIDE
15 1ONDANSETRON HYDROCHLORIDE AND DEXTROSE IN PLASTIC CONTAINER
16 1ONDANSETRON HYDROCHLORIDE DIHYDRATE INJECTION
17 20ONDANSETRON HYDROCHLORIDE PRESERVATIVE FREE
18 1ONDANSETRON INJECTION BP
19 3ONDANSETRON INJECTION USP
20 1ONDANSETRON INJECTION USP -(PRESERVATIVE FREE)
21 1ONDANSETRON INJECTION USP -(WITH PRESERVATIVE)
22 2OndaNish Inj
23 2OndanPol
24 3Ondancetron B. Braun
25 2Ondansetron
26 5Ondansetron Accord
27 2Ondansetron Accordpharma
28 1Ondansetron Aristo
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30 7Ondansetron Bluefish
31 1Ondansetron Cipla Tablets 4
32 1Ondansetron Cipla Tablets 8
33 2Ondansetron Farmalider
34 3Ondansetron Fresenius Kabi
35 1Ondansetron HCl
36 4Ondansetron Hameln
37 2Ondansetron Hikma
38 1Ondansetron Hydrochloride
39 2Ondansetron Ips
40 2Ondansetron Kabi
41 3Ondansetron Kalceks
42 4Ondansetron Normon
43 4Ondansetron Qualigen
44 2Ondansetron Ratio
45 2Ondansetron Serraclinics
46 2Ondansetron Teva-Ratio
47 2Ondansetron Viatris
48 1Ondron
49 2Otron
50 2PMS-ONDANSETRON
51 2SANDOZ ONDANSETRON
52 1Sabax Ondansetron injection 4mg/2ml
53 1Sabax Ondansetron injection 8mg/4ml
54 2TEVA-ONDANSETRON
55 1Vomigo
56 1Vomino
57 1Vomistop
58 1Vomiz D 4mg
59 1Vomiz D 8mg
60 5ZOFRAN
61 1ZOFRAN AND DEXTROSE IN PLASTIC CONTAINER
62 1ZOFRAN PRESERVATIVE FREE
63 1Zofer 4 Mg Injection
64 1Zofer 4 Mg Tablets
65 1Zofer 8 Mg Injection
66 1Zofer 8 Mg Tablets
67 1Zofer Rapitab 4
68 1Zofer Rapitab 8
69 19Zofran
70 2Zofran Zydis
71 8Blank
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01 39Canada
02 2France
03 11India
04 3Malta
05 33Norway
06 12South Africa
07 2South Korea
08 40Spain
09 3Turkey
10 102USA
11 1Vietnam
12 2Blank
Regulatory Info :
Registration Country : France
Brand Name : Ondansetron HCl
Dosage Form : Oro-Dispersible Tablet
Dosage Strength : 4MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info :
Registration Country : France
Brand Name : Ondansetron Hydrochloride
Dosage Form : Oro-Dispersible Tablet
Dosage Strength : 8MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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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Regulatory Info : DISCN
Registration Country : USA
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

Regulatory Info : DISCN
Registration Country : USA
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

Regulatory Info : RX
Registration Country : USA
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

Regulatory Info : RX
Registration Country : USA
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

Regulatory Info : DISCN
Registration Country : USA
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
