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 2EUGIA PHARMA INC.
15 3Fresenius Kabi USA
16 2GLAND PHARMA LIMITED
17 1GSK
18 3Glenmark Pharmaceuticals
19 3Glumex Pharmaceuticals Mfg. Pvt. Ltd
20 1Ha Noi CPC1 Pharmaceutical JSC
21 10Hikma Pharmaceuticals
22 6Hospira, Inc.
23 1Ind Swift Laboratories Limited
24 2Ipca Laboratories
25 3JAMP PHARMA
26 1Lannett Company, Inc.
27 1Luitpold Pharmaceuticals, Inc.
28 3MARCAN PHARMACEUTICALS INC
29 3MINT PHARMACEUTICALS INC
30 2Medipol Pharmaceutical
31 2Myungmoon Pharm. Co., LTD.
32 2Natco Pharma
33 2Natco Pharma (Canada) Inc
34 1Nishchem International Pvt. Ltd
35 1PHARM ASSOC
36 1PRO DOC LIMITEE
37 2Pharmascience Inc.
38 4Pliva Hrvatska
39 2Pluviaendo
40 1Polifarma
41 1Qilu Pharmaceutical
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 10Sun 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 14SOLUTION
14 7SOLUTION;ORAL
15 3Syrup
16 25TABLET
17 2TABLET; ORAL
18 42TABLET;ORAL
19 3Tablet
01 64DISCN
02 13Generic
03 36RX
04 59Blank
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 1Ondron
25 2Otron
26 2PMS-ONDANSETRON
27 2SANDOZ ONDANSETRON
28 1Sabax Ondansetron injection 4mg/2ml
29 1Sabax Ondansetron injection 8mg/4ml
30 2TEVA-ONDANSETRON
31 1Vomigo
32 1Vomino
33 1Vomistop
34 1Vomiz D 4mg
35 1Vomiz D 8mg
36 5ZOFRAN
37 1ZOFRAN AND DEXTROSE IN PLASTIC CONTAINER
38 1ZOFRAN PRESERVATIVE FREE
39 1Zofer 4 Mg Injection
40 1Zofer 4 Mg Tablets
41 1Zofer 8 Mg Injection
42 1Zofer 8 Mg Tablets
43 1Zofer Rapitab 4
44 1Zofer Rapitab 8
45 10Blank
01 39Canada
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
