Tentative Approval — This application has been tentatively approved by the FDA but is not yet listed in the Orange Book. It is blocked from final approval by unexpired patents or exclusivities on the reference listed drug.
DULOXETINE HYDROCHLORIDE
ANDATentative Approval
DULOXETINE HYDROCHLORIDE | A090775 | SANDOZ
Products (3)
Sort:
#001 — 20MG
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CAPSULE, DELAYED RELEASE; ORAL | TA Date: 2011-02-02 00:00:00
No patent or exclusivity listings for this strength.
#002 — 30MG
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CAPSULE, DELAYED RELEASE; ORAL | TA Date: 2011-02-02 00:00:00
#003 — 60MG
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CAPSULE, DELAYED RELEASE; ORAL | TA Date: 2011-02-02 00:00:00