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Active ingredient

Triamcinolone

266 finished FDA listings contain Triamcinolone as their only active ingredient; 36 combination products also contain it.

FDA NDC Directory

Ingredient names as written by FDA
TRIAMCINOLONE, TRIAMCINOLONE ACETONIDE, TRIAMCINOLONE DIACETATE, TRIAMCINOLONE HEXACETONIDE
Dosage forms
Aerosol, Spray, Cream, Injection, Suspension, Lotion, Ointment, Paste, Spray, Metered, Suspension
Routes
Dental, Intra-Arterial, Intra-Articular, Intralesional, Intramuscular, Nasal, Ophthalmic, Soft Tissue, Topical
Manufacturers / labelers
81
Strengths listed
.147 mg/g · .25 mg/g · .25 mg/ml · .5 mg/g · 1 mg/g · 1 mg/ml · 10 mg/ml · 200 mg/5ml · 40 mg/2ml · 40 mg/ml · 400 mg/10ml · 5 mg/g · 55 ug/1 · 80 mg/ml
Brand names in FDA listings
24 Hour Nasal Allergy, Allergy Nasal, Allergy Relief, Basic Care Nasal Allergy, Childrens Triamcinolone Acetonide, Dg Health Nasal Allergy, Equaline Nasal Allergy, Equate Nasal Allergy, Foster And Thrive 24 Hour Nasal Allergy, Good Neighbor Pharmacy 24 Hour Nasal Allergy, Good Sense Nasal Allergy, Hexatrione 2%, Kenalog-10, Kenalog-40, Kenalog-80, Kourzeq, Nasacort, Nasacort Allergy 24hr, Nasal Allergy, Nasal Allergy Relief, Oralone, Signature Care Nasal Allergy, Topcare Nasal Allergy, Triamcinolone Acetonide, Triamcinolone Acetonide Nasal, Triderm, Triesence, Triloan Ii Suik, Triloan Suik, Up And Up Nasal Allergy, Xipere

RxNorm (National Library of Medicine)

Ingredient concept RxCUI 10759

Drugs@FDA applications

Linked only where the FDA listing’s application number matches Drugs@FDA exactly. A listing in the NDC Directory does not by itself mean FDA approval.

ApplicationSponsorOriginal approvalListings
NDA 012041APOTHECON1960-01-042
NDA 014901APOTHECON1965-02-017
ANDA 085692FOUGERA PHARMS1978-03-099
ANDA 085691FOUGERA PHARMS1978-03-095
ANDA 086413PADAGIS US1981-04-0915
ANDA 087385PADAGIS US1981-11-0514
ANDA 088042CROWN LABS1984-03-1936
ANDA 070730SUN PHARMA CANADA1986-10-013
ANDA 089796COSETTE PHARMS NC1988-12-232
ANDA 089795COSETTE PHARMS NC1988-12-232
ANDA 040037SUN PHARMA CANADA1994-09-303
NDA 020468CHATTEM SANOFI1996-05-202
ANDA 040039TARO1997-11-264
ANDA 040671MICRO LABS2006-06-092
ANDA 040672MICRO LABS2006-12-132
NDA 022048HARROW EYE2007-11-292
ANDA 078104PERRIGO PHARMA INTL2009-07-3021
ANDA 040771RISING2010-07-013
ANDA 205373ENCUBE2016-05-132
ANDA 206379GLENMARK PHARMS LTD2016-07-222
ANDA 207117GLENMARK PHARMS LTD2016-08-051
ANDA 205592COSETTE PHARMS NC2017-01-122
ANDA 208590ENCUBE2017-03-032
ANDA 208320GLENMARK SPECLT2017-08-221
ANDA 208848ENCUBE2017-09-187
ANDA 207550AMNEAL2017-12-1119
ANDA 209535MACLEODS PHARMS2018-05-1825
ANDA 209852TEVA PHARMS USA2018-10-055
ANDA 209828MACLEODS PHARMS2018-11-2312
ANDA 212384ENCUBE2019-11-292
ANDA 213559QUAGEN2020-07-014
ANDA 212460PADAGIS ISRAEL2021-02-053
ANDA 213543LONG GROVE PHARMS2022-01-194
ANDA 212400EUGIA PHARMA2022-07-052
ANDA 212567MYLAN LABS LTD2022-11-023
ANDA 214582QUAGEN2022-12-092
ANDA 214615APOTEX2023-01-194
ANDA 218421DR REDDYS2025-04-113
ANDA 218601ALEMBIC2025-10-177
ANDA 220110AUROBINDO PHARMA LTD2026-08-112

Showing 40 of 51 applications.

Official labeling on DailyMed

Showing the 12 most recent of 209 labels.

Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.