APPLICATION
ANDA040555
TYPE
ANDA
ORIGINAL APPROVAL
2005-04-15
LATEST ACTION
2017-05-31
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued
Products
PHENTERMINE HYDROCHLORIDEDiscontinued
PHENTERMINE HYDROCHLORIDE 37.5MG · TABLET · ORAL
Approval history
2017-05-31Labeling · Supplement 16 · standardAP
2012-12-05Labeling · Supplement 10 · standardAP
2012-04-27Labeling · Supplement 9AP
2011-08-22Manufacturing (CMC) · Supplement 8AP
2005-04-15OriginalAP
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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