APPLICATION
ANDA088596
TYPE
ANDA
ORIGINAL APPROVAL
1984-04-04
LATEST ACTION
2000-07-26
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued
Products
PHENTERMINE HYDROCHLORIDEDiscontinued
PHENTERMINE HYDROCHLORIDE 37.5MG · TABLET · ORAL
Approval history
2000-07-26Manufacturing (CMC) · Supplement 18AP
1998-11-03Labeling · Supplement 17AP
1998-08-19Labeling · Supplement 16AP
1998-04-08Labeling · Supplement 15AP
1997-12-19Labeling · Supplement 14AP
1992-10-16Manufacturing (CMC) · Supplement 13AP
1991-01-31Labeling · Supplement 11AP
1990-05-24Labeling · Supplement 10AP
1989-12-15Labeling · Supplement 9AP
1989-06-15Labeling · Supplement 5AP
1989-06-15Labeling · Supplement 8AP
1988-06-27Manufacturing (CMC) · Supplement 6AP
1988-06-27Manufacturing (CMC) · Supplement 7AP
1986-05-22Manufacturing (CMC) · Supplement 2AP
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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