01 2ACCORD HLTHCARE
02 3AM REGENT
03 1AMNEAL PHARMS
04 2APOTEX
05 2APOTEX INC
06 4AUROBINDO PHARMA
07 2AVET LIFESCIENCES
08 2BAXTER HLTHCARE CORP
09 2CHARTWELL MOLECULAR
10 4CHARTWELL MOLECULES
11 3CHARTWELL RX
12 4DR REDDYS LABS LTD
13 2EUGIA PHARMA
14 3FRESENIUS KABI USA
15 2GLAND PHARMA LTD
16 1GLAXOSMITHKLINE
17 3GLENMARK PHARMS LTD
18 5HIKMA
19 2HIKMA FARMACEUTICA
20 3HIKMA INTL PHARMS
21 6HOSPIRA
22 2IPCA LABS LTD
23 1LANNETT CO INC
24 1LUITPOLD
25 2NATCO PHARMA LTD
26 1PHARM ASSOC
27 4PLIVA HRVATSKA DOO
28 1QILU PHARM HAINAN
29 5RISING
30 1SAGENT PHARMS
31 8SANDOZ
32 2STERISCIENCE SPECLTS
33 3SUN PHARM INDS (IN)
34 1SUN PHARM INDS LTD
35 4TARO
36 1TARO PHARMS IRELAND
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 : Yes
TE Code :
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Dosage Strength : EQ 0.64MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1995-01-31
Application Number : 20403
RX/OTC/DISCN : DISCN
RLD : Yes
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Dosage Strength : EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Dosage Strength : EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 :
RLD : Yes
TE Code :
Brand Name : ZOFRAN
Dosage Form : SOLUTION;ORAL
Dosage Strength : EQ 4MG BASE/5ML
Approval Date : 1997-01-24
Application Number : 20605
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : ONDANSETRON HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 24MG BASE
Approval Date : 2006-12-26
Application Number : 76183
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code : AB
Brand Name : ONDANSETRON HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 8MG BASE
Approval Date : 2006-12-26
Application Number : 76183
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : ONDANSETRON HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 4MG BASE
Approval Date : 2006-12-26
Application Number : 76183
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
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