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FDA NDA · NDA021929

BUDESONIDE AND FORMOTEROL FUMARATE DIHYDRATE

Sponsor: ASTRAZENECA

APPLICATION
NDA021929
TYPE
NDA
ORIGINAL APPROVAL
2006-07-21
LATEST ACTION
2017-12-20
ROUTE
RESPIRATORY (INHALATION), INHALATION
DOSAGE FORM
AEROSOL, METERED
MARKETING STATUS
Prescription

Products

SYMBICORT · ReferencePrescription
BUDESONIDE 0.16MG/INH, FORMOTEROL FUMARATE DIHYDRATE 0.0045MG/INH · AEROSOL, METERED · INHALATION
SYMBICORT · ReferencePrescription
BUDESONIDE 0.08MG/INH, FORMOTEROL FUMARATE DIHYDRATE 0.0045MG/INH · AEROSOL, METERED · INHALATION

Approval history

2017-12-20Efficacy · Supplement 42 · standardLabelAP
2017-09-11Efficacy · Supplement 41 · standardLabelAP
2017-01-27Efficacy · Supplement 13 · unknownLabelAP
2016-06-10Manufacturing (CMC) · Supplement 40 · standardAP
2015-04-14Manufacturing (CMC) · Supplement 38 · standardAP
2014-06-28Manufacturing (CMC) · Supplement 39 · standardAP
2014-04-04Manufacturing (CMC) · Supplement 37 · standardAP
2014-02-27Manufacturing (CMC) · Supplement 36 · standardAP
2014-01-15Manufacturing (CMC) · Supplement 35 · standardAP
2012-07-23REMS · Supplement 33LetterAP
2012-05-08Manufacturing (CMC) · Supplement 30AP
2011-08-18REMS · Supplement 28LetterAP
2011-02-16REMS · Supplement 19LetterAP
2010-06-25Labeling · Supplement 21 · 901 orderLabelAP
2009-02-27Efficacy · Supplement 12 · standardReviewAP
2008-07-16Labeling · Supplement 10 · standardLabelAP
2007-10-31Labeling · Supplement 4 · standardLabelAP
2007-10-26Manufacturing (CMC) · Supplement 6 · standardLetterAP
2006-07-21Type 4 - New Combination · Original · standardLabelAP
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