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

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01 2Ampoule
02 1CAPSULE; ORAL
03 4DSP
04 2FCT
05 28Film Coated Tablet
06 4INJ
07 50INJECTABLE;INJECTION
08 3INJECTION
09 1Injectable And Infusion Solution
10 2Injectable And Infusion Solution In Pre-Filled Syringe
11 1Injectable And Perfusion Solution
12 17Injectable Solution
13 2Injection
14 1Injection / Infusion Solution
15 2ORALLY DISINTEGRATING TABLET
16 2Oral Lyophilized
17 1Oral Solution
18 2Oro-Dispersible Tablet
19 14SOLUTION
20 6SOLUTION;ORAL
21 10Solution For Injection
22 1Solution For Injection And Infusion
23 6Solution For Injection/Infusion
24 4Solution For Perfusion
25 7Syrup
26 2TAB
27 25TABLET
28 2TABLET; ORAL
29 40TABLET;ORAL
30 5Tablet
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01 1Authorised
02 33Authorized
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04 62DISCN
05 15Generic
06 29Marketed
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08 39PRESCRIPTION
09 34RX
10 2Withdrawn
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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 1LOSARTAN POTASSIUM
08 2MAR-ONDANSETRON
09 2MINT-ONDANSETRON
10 1MINT-ONDANSETRON SOLUTION
11 2MYLAN-ONDANSETRON
12 2NAT-ONDANSETRON
13 1Nausazy
14 5ONDANSETRON
15 70ONDANSETRON HYDROCHLORIDE
16 1ONDANSETRON HYDROCHLORIDE AND DEXTROSE IN PLASTIC CONTAINER
17 1ONDANSETRON HYDROCHLORIDE DIHYDRATE INJECTION
18 19ONDANSETRON HYDROCHLORIDE PRESERVATIVE FREE
19 1ONDANSETRON INJECTION BP
20 3ONDANSETRON INJECTION USP
21 1ONDANSETRON INJECTION USP -(PRESERVATIVE FREE)
22 1ONDANSETRON INJECTION USP -(WITH PRESERVATIVE)
23 2OndaNish Inj
24 2OndanPol
25 3Ondancetron B. Braun
26 2Ondansetron
27 5Ondansetron Accord
28 2Ondansetron Accordpharma
29 1Ondansetron Aristo
30 1Ondansetron Aurovitas
31 7Ondansetron Bluefish
32 1Ondansetron Cipla Tablets 4
33 1Ondansetron Cipla Tablets 8
34 2Ondansetron Farmalider
35 3Ondansetron Fresenius Kabi
36 1Ondansetron HCl
37 4Ondansetron Hameln
38 2Ondansetron Hikma
39 1Ondansetron Hydrochloride
40 2Ondansetron Ips
41 2Ondansetron Kabi
42 3Ondansetron Kalceks
43 4Ondansetron Normon
44 4Ondansetron Qualigen
45 2Ondansetron Ratio
46 2Ondansetron Serraclinics
47 2Ondansetron Teva-Ratio
48 2Ondansetron Viatris
49 1Ondron
50 2Otron
51 2PMS-ONDANSETRON
52 2SANDOZ ONDANSETRON
53 1STAVUDINE
54 1Sabax Ondansetron injection 4mg/2ml
55 1Sabax Ondansetron injection 8mg/4ml
56 2TEVA-ONDANSETRON
57 1Vomigo
58 1Vomino
59 1Vomistop
60 1Vomiz D 4mg
61 1Vomiz D 8mg
62 5ZOFRAN
63 1ZOFRAN AND DEXTROSE IN PLASTIC CONTAINER
64 1ZOFRAN PRESERVATIVE FREE
65 1Zofer 4 Mg Injection
66 1Zofer 4 Mg Tablets
67 1Zofer 8 Mg Injection
68 1Zofer 8 Mg Tablets
69 1Zofer Rapitab 4
70 1Zofer Rapitab 8
71 19Zofran
72 2Zofran Zydis
73 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 99USA
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
