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FDA ANDA · ANDA076332

FLUCONAZOLE

Sponsor: SUN PHARM INDS LTD

APPLICATION
ANDA076332
TYPE
ANDA
ORIGINAL APPROVAL
2004-07-29
LATEST ACTION
2008-10-03
ROUTE
ORAL
DOSAGE FORM
FOR SUSPENSION
MARKETING STATUS
Discontinued

Products

FLUCONAZOLEDiscontinued
FLUCONAZOLE 200MG/5ML · FOR SUSPENSION · ORAL
FLUCONAZOLEDiscontinued
FLUCONAZOLE 50MG/5ML · FOR SUSPENSION · ORAL

Approval history

2008-10-03Labeling · Supplement 5AP
2004-07-29OriginalLetterAP
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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