01 4TARO
02 1TARO PHARMS IRELAND
03 2ACCORD HLTHCARE
04 3AM REGENT
05 1AMNEAL PHARMS
06 2APOTEX
07 2APOTEX INC
08 4AUROBINDO PHARMA
09 2AVET LIFESCIENCES
10 2BAXTER HLTHCARE CORP
11 2CHARTWELL MOLECULAR
12 4CHARTWELL MOLECULES
13 3CHARTWELL RX
14 4DR REDDYS LABS LTD
15 2EUGIA PHARMA
16 3FRESENIUS KABI USA
17 2GLAND PHARMA LTD
18 1GLAXOSMITHKLINE
19 3GLENMARK PHARMS LTD
20 5HIKMA
21 2HIKMA FARMACEUTICA
22 3HIKMA INTL PHARMS
23 6HOSPIRA
24 2IPCA LABS LTD
25 1LANNETT CO INC
26 1LUITPOLD
27 2NATCO PHARMA LTD
28 1PHARM ASSOC
29 4PLIVA HRVATSKA DOO
30 1QILU PHARM HAINAN
31 5RISING
32 1SAGENT PHARMS
33 8SANDOZ
34 2STERISCIENCE SPECLTS
35 3SUN PHARM INDS (IN)
36 1SUN PHARM INDS LTD
37 5TEVA
38 2WOCKHARDT
01 51INJECTABLE;INJECTION
02 7SOLUTION;ORAL
03 2TABLET; ORAL
04 42TABLET;ORAL
01 60DISCN
02 40RX
03 2Blank
01 74ONDANSETRON HYDROCHLORIDE
02 1ONDANSETRON HYDROCHLORIDE AND DEXTROSE IN PLASTIC CONTAINER
03 20ONDANSETRON HYDROCHLORIDE PRESERVATIVE FREE
04 5ZOFRAN
05 1ZOFRAN AND DEXTROSE IN PLASTIC CONTAINER
06 1ZOFRAN PRESERVATIVE FREE
01 93No
02 7Yes
03 2Blank
RLD : No
TE Code :
Brand Name : ONDANSETRON HYDROCHLORIDE
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 4MG BASE/5ML
Approval Date : 2007-11-30
Application Number : 77009
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : ONDANSETRON HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 4MG BASE
Approval Date : 2011-03-28
Application Number : 77729
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : ONDANSETRON HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 8MG BASE
Approval Date : 2011-03-28
Application Number : 77729
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : ONDANSETRON HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 24MG BASE
Approval Date : 2011-03-28
Application Number : 77729
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : ONDANSETRON HYDROCHLORIDE PRESERVATIVE FREE
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 2MG BASE/ML
Approval Date : 2008-03-21
Application Number : 78014
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
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Dosage Strength : EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1991-01-04
Application Number : 20007
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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**
Approval Date : 1993-12-10
Application Number : 20007
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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**
Approval Date : 1992-12-31
Application Number : 20103
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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**
Approval Date : 1992-12-31
Application Number : 20103
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
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**
Approval Date : 1999-08-27
Application Number : 20103
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
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