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FDA NDA · NDA202278

ZECUITY

Sponsor: TEVA BRANDED PHARM

APPLICATION
NDA202278
TYPE
NDA
ORIGINAL APPROVAL
2013-01-17
LATEST ACTION
2015-08-24
ROUTE
IONTOPHORESIS
DOSAGE FORM
SYSTEM
MARKETING STATUS
Discontinued

Products

ZECUITY · ReferenceDiscontinued
SUMATRIPTAN SUCCINATE EQ 6.5MG BASE/4HR · SYSTEM · IONTOPHORESIS

Approval history

2015-08-24Manufacturing (CMC) · Supplement 6 · standardAP
2015-04-07Manufacturing (CMC) · Supplement 7 · standardAP
2015-03-16Manufacturing (CMC) · Supplement 3 · standardAP
2014-03-21Labeling · Supplement 2 · standardLabelAP
2014-03-21Labeling · Supplement 1 · standardLabelAP
2014-01-17Manufacturing (CMC) · Supplement 4 · standardAP
2013-01-17Type 3 - New Dosage Form · Original · standardLabelAP
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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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