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FDA NDA · NDA019143

ALPHATREX

Sponsor: SAVAGE LABS

APPLICATION
NDA019143
TYPE
NDA
ORIGINAL APPROVAL
1984-09-04
LATEST ACTION
1996-11-01
ROUTE
TOPICAL
DOSAGE FORM
OINTMENT
MARKETING STATUS
Discontinued

Products

ALPHATREXDiscontinued
BETAMETHASONE DIPROPIONATE EQ 0.05% BASE · OINTMENT · TOPICAL

Approval history

1996-11-01Labeling · Supplement 12AP
1996-06-13Manufacturing (CMC) · Supplement 11AP
1996-03-07Manufacturing (CMC) · Supplement 13AP
1992-07-16Manufacturing (CMC) · Supplement 10AP
1988-11-01Manufacturing (CMC) · Supplement 9AP
1988-11-01Manufacturing (CMC) · Supplement 7AP
1988-11-01Manufacturing (CMC) · Supplement 8AP
1987-10-20Manufacturing (CMC) · Supplement 4AP
1987-07-06Manufacturing (CMC) · Supplement 5AP
1987-05-29Manufacturing (CMC) · Supplement 6AP
1986-06-27Manufacturing (CMC) · Supplement 2AP
1986-03-28Manufacturing (CMC) · Supplement 1AP
1984-09-04OriginalAP
VIEW ON DRUGS@FDA ↗

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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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