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FDA ANDA · ANDA205468

VENLAFAXINE HYDROCHLORIDE

Sponsor: MPP PHARMA

APPLICATION
ANDA205468
TYPE
ANDA
ORIGINAL APPROVAL
2017-03-24
LATEST ACTION
2017-03-24
ROUTE
ORAL
DOSAGE FORM
TABLET, EXTENDED RELEASE
MARKETING STATUS
Prescription

Products

VENLAFAXINE HYDROCHLORIDEPrescription
VENLAFAXINE HYDROCHLORIDE EQ 150MG BASE · TABLET, EXTENDED RELEASE · ORAL
VENLAFAXINE HYDROCHLORIDEPrescription
VENLAFAXINE HYDROCHLORIDE EQ 225MG BASE · TABLET, EXTENDED RELEASE · ORAL

Approval history

2017-03-24UNKNOWN · Original · standardLetterAP
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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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