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FDA ANDA · ANDA090723

DULOXETINE

duloxetine hydrochloride

Sponsor: ADAPTIS

APPLICATION
ANDA090723
TYPE
ANDA
ORIGINAL APPROVAL
2013-12-11
LATEST ACTION
2014-12-04
ROUTE
ORAL
DOSAGE FORM
CAPSULE, DELAYED REL PELLETS
MARKETING STATUS
Discontinued

Products

DULOXETINE HYDROCHLORIDEDiscontinued
DULOXETINE HYDROCHLORIDE EQ 30MG BASE · CAPSULE, DELAYED REL PELLETS · ORAL
DULOXETINE HYDROCHLORIDEDiscontinued
DULOXETINE HYDROCHLORIDE EQ 60MG BASE · CAPSULE, DELAYED REL PELLETS · ORAL
DULOXETINE HYDROCHLORIDEDiscontinued
DULOXETINE HYDROCHLORIDE EQ 20MG BASE · CAPSULE, DELAYED REL PELLETS · ORAL

Approval history

2014-12-04Labeling · Supplement 1 · standardAP
2013-12-11OriginalLetterAP
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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