APPLICATION
NDA019591
TYPE
NDA
ORIGINAL APPROVAL
1989-05-02
LATEST ACTION
2011-04-29
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued
Products
LARIAM · ReferenceDiscontinued
MEFLOQUINE HYDROCHLORIDE 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TABLET · ORAL
Approval history
2002-06-21Manufacturing (CMC) · Supplement 18 · standardAP
2002-03-24Manufacturing (CMC) · Supplement 15 · standardAP
1999-11-10Manufacturing (CMC) · Supplement 13 · standardAP
1999-08-02Labeling · Supplement 12 · standardAP
1999-08-02Labeling · Supplement 10 · standardAP
1998-10-20Manufacturing (CMC) · Supplement 11 · standardAP
1997-08-06Labeling · Supplement 7 · standardAP
1996-01-22Manufacturing (CMC) · Supplement 9 · standardAP
1995-06-16Manufacturing (CMC) · Supplement 8 · standardAP
1993-11-03Manufacturing (CMC) · Supplement 6 · standardAP
1993-11-02Labeling · Supplement 5 · standardAP
1992-11-23Efficacy · Supplement 3 · standardAP
1991-10-04Manufacturing (CMC) · Supplement 4 · standardAP
1990-07-30Manufacturing (CMC) · Supplement 2 · standardAP
1990-02-02Labeling · Supplement 1 · standardAP
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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