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FDA ANDA · ANDA087798

TRIAMCINOLONE ACETONIDE

Sponsor: ACTAVIS MID ATLANTIC

APPLICATION
ANDA087798
TYPE
ANDA
ORIGINAL APPROVAL
1982-06-04
LATEST ACTION
2001-05-30
ROUTE
TOPICAL
DOSAGE FORM
CREAM
MARKETING STATUS
Discontinued

Products

TRIAMCINOLONE ACETONIDEDiscontinued
TRIAMCINOLONE ACETONIDE 0.1% · CREAM · TOPICAL

Approval history

2001-05-30Manufacturing (CMC) · Supplement 24AP
2000-12-29Manufacturing (CMC) · Supplement 23AP
2000-09-25Manufacturing (CMC) · Supplement 22AP
1997-06-23Manufacturing (CMC) · Supplement 19AP
1997-06-23Manufacturing (CMC) · Supplement 17AP
1997-06-23Manufacturing (CMC) · Supplement 18AP
1997-06-23Manufacturing (CMC) · Supplement 16AP
1997-05-12Manufacturing (CMC) · Supplement 21AP
1996-06-28Manufacturing (CMC) · Supplement 20AP
1996-02-07Manufacturing (CMC) · Supplement 15AP
1995-07-24Manufacturing (CMC) · Supplement 14AP
1991-02-11Labeling · Supplement 13AP
1989-07-26Manufacturing (CMC) · Supplement 11AP
1989-07-26Manufacturing (CMC) · Supplement 12AP
1988-06-15Manufacturing (CMC) · Supplement 7AP
1988-06-15Manufacturing (CMC) · Supplement 9AP
1985-12-20Manufacturing (CMC) · Supplement 5AP
1983-03-31Manufacturing (CMC) · Supplement 4AP
1983-03-21Manufacturing (CMC) · Supplement 3AP
1983-02-14Manufacturing (CMC) · Supplement 1AP
1982-06-04OriginalAP
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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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