01 2ALKEM LABS LTD
02 2ANDA REPOSITORY
03 2AUROBINDO PHARMA
04 2AUROBINDO PHARMA LTD
05 2CHARTWELL RX
06 4PHARMACIA AND UPJOHN
07 2SANDOZ
08 4SANKYO
09 4SUN PHARM INDS LTD
01 10FOR SUSPENSION;ORAL
02 14TABLET;ORAL
01 14DISCN
02 10RX
01 4BANAN
02 16CEFPODOXIME PROXETIL
03 4VANTIN
01 20No
02 4Yes
RLD : No
TE Code :
Brand Name : BANAN
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 100MG BASE
Approval Date : 1992-08-07
Application Number : 50687
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : BANAN
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 200MG BASE
Approval Date : 1992-08-07
Application Number : 50687
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : BANAN
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 100MG BASE/5ML
Approval Date : 1992-08-07
Application Number : 50688
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : BANAN
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 50MG BASE/5ML
Approval Date : 1992-08-07
Application Number : 50688
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : VANTIN
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1992-08-07
Application Number : 50674
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : VANTIN
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1992-08-07
Application Number : 50674
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : VANTIN
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 50MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1992-08-07
Application Number : 50675
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code :
Brand Name : VANTIN
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 100MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1992-08-07
Application Number : 50675
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : CEFPODOXIME PROXETIL
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 50MG BASE/5ML
Approval Date : 2002-05-31
Application Number : 65082
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
RLD : No
TE Code :
Brand Name : CEFPODOXIME PROXETIL
Dosage Form : FOR SUSPENSION;ORAL
Dosage Strength : EQ 100MG BASE/5ML
Approval Date : 2002-05-31
Application Number : 65082
RX/OTC/DISCN : DISCN
RLD : No
TE Code :
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