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FDA ANDA · ANDA078751

NARATRIPTAN

Sponsor: ANI PHARMS

APPLICATION
ANDA078751
TYPE
ANDA
ORIGINAL APPROVAL
2010-07-07
LATEST ACTION
2015-07-15
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

NARATRIPTANDiscontinued
NARATRIPTAN HYDROCHLORIDE EQ 2.5MG BASE · TABLET · ORAL
NARATRIPTANDiscontinued
NARATRIPTAN HYDROCHLORIDE EQ 1MG BASE · TABLET · ORAL

Approval history

2015-07-15Labeling · Supplement 5 · standardAP
2012-04-24Labeling · Supplement 2AP
2010-12-30Labeling · Supplement 1AP
2010-07-07OriginalLetterAP
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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