APPLICATION
ANDA084343
TYPE
ANDA
ORIGINAL APPROVAL
1974-07-16
LATEST ACTION
1992-11-09
ROUTE
TOPICAL
DOSAGE FORM
LOTION
MARKETING STATUS
Discontinued
Products
KENALOGDiscontinued
TRIAMCINOLONE ACETONIDE 0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · LOTION · TOPICAL
KENALOGDiscontinued
TRIAMCINOLONE ACETONIDE 0.025% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · LOTION · TOPICAL
Approval history
1992-11-09Manufacturing (CMC) · Supplement 31AP
1983-06-28Manufacturing (CMC) · Supplement 25AP
1983-05-05Manufacturing (CMC) · Supplement 24AP
1982-12-01Manufacturing (CMC) · Supplement 23AP
1982-06-21Manufacturing (CMC) · Supplement 22AP
1981-12-21Manufacturing (CMC) · Supplement 17AP
1981-12-21Manufacturing (CMC) · Supplement 21AP
1981-12-21Manufacturing (CMC) · Supplement 18AP
1974-07-16OriginalAP
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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