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FDA NDA · NDA050791

MYFORTIC

mycophenolic acid

Sponsor: NOVARTIS

APPLICATION
NDA050791
TYPE
NDA
ORIGINAL APPROVAL
2004-02-27
LATEST ACTION
2026-07-29
ROUTE
ORAL
DOSAGE FORM
TABLET, DELAYED RELEASE
MARKETING STATUS
Prescription

Products

MYFORTIC · ReferencePrescription
MYCOPHENOLATE SODIUM EQ 360MG BASE · TABLET, DELAYED RELEASE · ORAL
MYFORTIC · ReferencePrescription
MYCOPHENOLATE SODIUM EQ 180MG BASE · TABLET, DELAYED RELEASE · ORAL

Approval history

2026-07-29REMS · Supplement 43LetterAP
2026-07-29Labeling · Supplement 42 · standardLetterAP
2025-06-27Labeling · Supplement 40 · standardLetterAP
2024-08-13REMS · Supplement 38LetterAP
2022-03-15Labeling · Supplement 35 · standardLetterAP
2021-08-11REMS · Supplement 36LetterAP
2021-04-21REMS · Supplement 34LetterAP
2021-01-15REMS · Supplement 33LetterAP
2020-11-03Manufacturing (CMC) · Supplement 32LetterAP
2020-04-28Labeling · Supplement 30 · standardLetterAP
2015-12-23Manufacturing (CMC) · Supplement 23 · standardAP
2015-11-13REMS · Supplement 22LetterAP
2015-10-27Labeling · Supplement 24 · standardLabelAP
2015-08-04Manufacturing (CMC) · Supplement 21 · standardLetterAP
2013-09-27Labeling · Supplement 18 · standardLabelAP
2013-09-27REMS · Supplement 19LetterAP
2013-05-01Manufacturing (CMC) · Supplement 16 · standardAP
2013-05-01Labeling · Supplement 12 · standardLabelAP
2013-02-08Manufacturing (CMC) · Supplement 15 · standardAP
2012-09-25Labeling · Supplement 5 · standardLetterAP
2012-06-22Labeling · Supplement 14 · standardLabelAP
2010-10-27Labeling · Supplement 11 · unknownLabelAP
2009-10-08Labeling · Supplement 8 · unknownLabelAP
2009-07-10Labeling · Supplement 7 · standardLabelAP
2009-03-27Labeling · Supplement 6 · standardLetterAP
2008-12-15Labeling · Supplement 4 · standardLabelAP
2008-05-09Labeling · Supplement 2 · standardLabelAP
2007-11-02Labeling · Supplement 1 · standardLabelAP
2004-02-27Type 2 - New Active Ingredient · Original · standardOther Important Information from FDAAP
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