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

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01 2Ampoule
02 4DSP
03 2FCT
04 15Film 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 1Solution For Injection And Infusion
21 4Solution For Perfusion
22 5Syrup
23 2TAB
24 25TABLET
25 2TABLET; ORAL
26 42TABLET;ORAL
27 3Tablet
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01 1Authorised
02 33Authorized
03 7Cancelled
04 65DISCN
05 15Generic
06 39Prescription
07 35RX
08 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 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 3Ondansetron Accord
27 1Ondansetron Aristo
28 1Ondansetron Aurovitas
29 1Ondansetron Cipla Tablets 4
30 1Ondansetron Cipla Tablets 8
31 2Ondansetron Farmalider
32 1Ondansetron Fresenius Kabi
33 1Ondansetron HCl
34 2Ondansetron Hikma
35 1Ondansetron Hydrochloride
36 2Ondansetron Ips
37 2Ondansetron Kabi
38 1Ondansetron Kalceks
39 4Ondansetron Normon
40 4Ondansetron Qualigen
41 2Ondansetron Ratio
42 2Ondansetron Serraclinics
43 2Ondansetron Teva-Ratio
44 2Ondansetron Viatris
45 1Ondron
46 2Otron
47 2PMS-ONDANSETRON
48 2SANDOZ ONDANSETRON
49 1Sabax Ondansetron injection 4mg/2ml
50 1Sabax Ondansetron injection 8mg/4ml
51 2TEVA-ONDANSETRON
52 1Vomigo
53 1Vomino
54 1Vomistop
55 1Vomiz D 4mg
56 1Vomiz D 8mg
57 5ZOFRAN
58 1ZOFRAN AND DEXTROSE IN PLASTIC CONTAINER
59 1ZOFRAN PRESERVATIVE FREE
60 1Zofer 4 Mg Injection
61 1Zofer 4 Mg Tablets
62 1Zofer 8 Mg Injection
63 1Zofer 8 Mg Tablets
64 1Zofer Rapitab 4
65 1Zofer Rapitab 8
66 5Zofran
67 2Zofran Zydis
68 8Blank
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01 39Canada
02 2France
03 11India
04 3Malta
05 12South Africa
06 2South Korea
07 40Spain
08 3Turkey
09 102USA
10 1Vietnam
11 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
