APPLICATION
NDA012104
TYPE
NDA
ORIGINAL APPROVAL
1974-10-11
LATEST ACTION
2017-01-26
ROUTE
TOPICAL
DOSAGE FORM
SPRAY
MARKETING STATUS
Discontinued
Products
KENALOG · ReferenceDiscontinued
TRIAMCINOLONE ACETONIDE 0.147MG/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · SPRAY · TOPICAL
Approval history
2017-01-26Manufacturing (CMC) · Supplement 37 · standardAP
2015-10-06Manufacturing (CMC) · Supplement 36 · standardAP
2013-11-15Manufacturing (CMC) · Supplement 35 · standardAP
2013-06-21Manufacturing (CMC) · Supplement 34 · standardAP
2009-08-20Manufacturing (CMC) · Supplement 30AP
2001-10-12Manufacturing (CMC) · Supplement 28 · standardAP
1997-03-05Manufacturing (CMC) · Supplement 27 · standardAP
1992-09-23Manufacturing (CMC) · Supplement 26 · standardAP
1987-06-04Manufacturing (CMC) · Supplement 25 · standardAP
1985-08-23Manufacturing (CMC) · Supplement 24 · standardAP
1985-06-11Manufacturing (CMC) · Supplement 23 · standardAP
1983-10-06Manufacturing (CMC) · Supplement 22 · standardAP
1982-08-20Labeling · Supplement 21AP
1980-07-21Manufacturing (CMC) · Supplement 20 · standardAP
1979-10-02Labeling · Supplement 19AP
1979-03-16Manufacturing (CMC) · Supplement 18 · standardAP
1978-07-05Labeling · Supplement 17AP
1977-10-11Manufacturing (CMC) · Supplement 15 · standardAP
1977-10-11Manufacturing (CMC) · Supplement 14 · standardAP
1977-06-23Labeling · Supplement 13AP
1977-02-04Manufacturing (CMC) · Supplement 12 · standardAP
1976-10-18Labeling · Supplement 11AP
1974-10-11Type 3 - New Dosage Form · Original · standardAP
1974-10-11Manufacturing (CMC) · Supplement 9 · standardAP
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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