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FDA ANDA · ANDA076786

DONEPEZIL HYDROCHLORIDE

Sponsor: SUN PHARM INDS LTD

APPLICATION
ANDA076786
TYPE
ANDA
ORIGINAL APPROVAL
2010-11-26
LATEST ACTION
2014-08-14
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

DONEPEZIL HYDROCHLORIDEDiscontinued
DONEPEZIL HYDROCHLORIDE 10MG · TABLET · ORAL
DONEPEZIL HYDROCHLORIDEDiscontinued
DONEPEZIL HYDROCHLORIDE 5MG · TABLET · ORAL

Approval history

2014-08-14Labeling · Supplement 6 · standardAP
2011-02-16Labeling · Supplement 1AP
2011-02-16Labeling · Supplement 2AP
2010-11-26OriginalLetterAP
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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