Athena Pharmaceutiques is a Partner of Choice for Drug Delivery & Life Cycle Management.
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 3Fresenius Kabi USA
15 2GLAND PHARMA LIMITED
16 1GSK
17 3Glenmark Pharmaceuticals
18 3Glumex Pharmaceuticals Mfg. Pvt. Ltd
19 1Ha Noi CPC1 Pharmaceutical JSC
20 10Hikma Pharmaceuticals
21 6Hospira, Inc.
22 1Ind Swift Laboratories Limited
23 2Ipca Laboratories
24 3JAMP PHARMA
25 1Lannett Company, Inc.
26 1Luitpold Pharmaceuticals, Inc.
27 3MARCAN PHARMACEUTICALS INC
28 2MINT PHARMACEUTICALS INC
29 2Medipol Pharmaceutical
30 2Myungmoon Pharm. Co., LTD.
31 2Natco Pharma
32 2Natco Pharma (Canada) Inc
33 1Nishchem International Pvt. Ltd
34 1PHARM ASSOC
35 1PRO DOC LIMITEE
36 2Pharmascience Inc.
37 4Pliva Hrvatska
38 2Pluviaendo
39 1Polifarma
40 1Qilu Pharmaceutical
41 6RANBAXY LABORATORIES LIMITED
42 5Rising Pharmaceuticals Inc
43 2SANIS HEALTH INC
44 2SIVEM PHARMACEUTICALS ULC
45 2STERIMAX INC
46 2STERISCIENCE SPECLTS
47 1Sagent Pharmaceuticals
48 13Sandoz B2B
49 2Smith & Kenner Pharmaceuticals
50 4Sun Pharmaceutical Industries Limited
51 5Taro Pharmaceutical Industries
52 7Teva Pharmaceutical Industries
53 1Unicor Pharmatech
54 2Viatris
55 2Wockhardt
56 4XYZ Pharma
57 2Zydus Lifesciences
58 1Blank
01 2Ampoule
02 4DSP
03 2FCT
04 2Film Coated Tablet
05 4INJ
06 51INJECTABLE;INJECTION
07 3INJECTION
08 2Injection
09 1Injection / Infusion Solution
10 2ORALLY DISINTEGRATING TABLET
11 1Oral Solution
12 2Oro-Dispersible Tablet
13 11SOLUTION
14 7SOLUTION;ORAL
15 3Syrup
16 25TABLET
17 2TABLET; ORAL
18 42TABLET;ORAL
19 3Tablet
01 60DISCN
02 13Generic
03 36Prescription
04 40RX
05 20Blank
01 2ACCEL-ONDANSETRON
02 3APO-ONDANSETRON
03 2AURO-ONDANSETRON INJECTION
04 1JAMP ONDANSETRON
05 2JAMP-ONDANSETRON
06 2MAR-ONDANSETRON
07 2MINT-ONDANSETRON
08 2MYLAN-ONDANSETRON
09 2NAT-ONDANSETRON
10 1Nausazy
11 5ONDANSETRON
12 74ONDANSETRON HYDROCHLORIDE
13 1ONDANSETRON HYDROCHLORIDE AND DEXTROSE IN PLASTIC CONTAINER
14 1ONDANSETRON HYDROCHLORIDE DIHYDRATE INJECTION
15 20ONDANSETRON HYDROCHLORIDE PRESERVATIVE FREE
16 1ONDANSETRON INJECTION BP
17 3ONDANSETRON INJECTION USP
18 1ONDANSETRON INJECTION USP -(PRESERVATIVE FREE)
19 1ONDANSETRON INJECTION USP -(WITH PRESERVATIVE)
20 2OndaNish Inj
21 2OndanPol
22 1Ondron
23 2Otron
24 2PMS-ONDANSETRON
25 2SANDOZ ONDANSETRON
26 1Sabax Ondansetron injection 4mg/2ml
27 1Sabax Ondansetron injection 8mg/4ml
28 2TEVA-ONDANSETRON
29 1Vomigo
30 1Vomino
31 1Vomistop
32 1Vomiz D 4mg
33 1Vomiz D 8mg
34 5ZOFRAN
35 1ZOFRAN AND DEXTROSE IN PLASTIC CONTAINER
36 1ZOFRAN PRESERVATIVE FREE
37 1Zofer 4 Mg Injection
38 1Zofer 4 Mg Tablets
39 1Zofer 8 Mg Injection
40 1Zofer 8 Mg Tablets
41 1Zofer Rapitab 4
42 1Zofer Rapitab 8
43 10Blank
01 36Canada
02 2France
03 11India
04 10South Africa
05 2South Korea
06 3Turkey
07 102USA
08 1Vietnam
09 2Blank
Athena Pharmaceutiques is a Partner of Choice for Drug Delivery & Life Cycle Management.
Regulatory Info :
Registration Country : France
Brand Name :
Dosage Form : Oro-Dispersible Tablet
Dosage Strength : 4MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Athena Pharmaceutiques is a Partner of Choice for Drug Delivery & Life Cycle Management.
Regulatory Info :
Registration Country : France
Brand Name :
Dosage Form : Oro-Dispersible Tablet
Dosage Strength : 8MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : France
Regulatory Info : RX
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 : 76972
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
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 : 76974
Regulatory Info : RX
Registration Country : USA
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
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
Regulatory Info : RX
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 : 76781
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ONDANSETRON HYDROCHLORIDE
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 4MG BASE/5ML
Packaging :
Approval Date : 2006-12-26
Application Number : 76960
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
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 : 76967
Regulatory Info : RX
Registration Country : USA
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
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
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 : 76930
Regulatory Info : DISCN
Registration Country : USA
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 : 76930
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : ONDANSETRON HYDROCHLORIDE
Dosage Form : TABLET; ORAL
Dosage Strength : EQ 16MG
Packaging :
Approval Date :
Application Number : 76930
Regulatory Info :
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 : 2007-06-25
Application Number : 76930
Regulatory Info : DISCN
Registration Country : USA
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
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
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
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
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
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ZOFRAN
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 4MG BASE/5ML
Packaging :
Approval Date : 1997-01-24
Application Number : 20605
Regulatory Info : DISCN
Registration Country : USA
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
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
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
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 : INJECTABLE;INJECTION
Dosage Strength : EQ 2MG BASE/ML
Packaging :
Approval Date : 2006-11-22
Application Number : 76876
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
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