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FDA ANDA · ANDA065083

CEFPODOXIME PROXETIL

Sponsor: SUN PHARM INDS LTD

APPLICATION
ANDA065083
TYPE
ANDA
ORIGINAL APPROVAL
2003-08-20
LATEST ACTION
2008-04-25
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

CEFPODOXIME PROXETILDiscontinued
CEFPODOXIME PROXETIL EQ 200MG BASE · TABLET · ORAL
CEFPODOXIME PROXETILDiscontinued
CEFPODOXIME PROXETIL EQ 100MG BASE · TABLET · ORAL

Approval history

2008-04-25Labeling · Supplement 10AP
2004-07-12Labeling · Supplement 2AP
2003-08-20OriginalAP
VIEW ON DRUGS@FDA ↗

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Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

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