Home NDC 76420-222-01 Triloan II SUIK
Product NDC 76420-222
Requested package NDC 76420-222-01
11-digit product format 764200222
Labeler code 76420
Product ID 76420-222_0e7fdebd-8ab4-024a-e063-6394a90afec3
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Triamcinolone Acetonide
Dosage form INJECTION, SUSPENSION
Route INTRA-ARTICULAR; INTRAMUSCULAR
Labeler Asclemed USA, Inc.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2009-06-01
Substance TRIAMCINOLONE ACETONIDE
Active strength 40 mg/mL
Pharmacologic classes Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Triloan II SUIK
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TRIAMCINOLONE ACETONIDE 40 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination F446C597KA Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 76420-222-01 Triloan II SUIK 2 in 1 CARTON INJECTION, SUSPENSION 2 9 76420-222-01 Triloan II SUIK 1 mL in 1 VIAL, SINGLE-DOSE INJECTION, SUSPENSION 1 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76420-222 TRILOAN II SUIK (TRIAMCINOLONE ACETONIDE) INJECTION, SUSPENSION [ASCLEMED USA, INC.] 9 Current NDC, Legacy NDC, 2 package rows 20240110_af3d002d-5e8e-44f6-bdd9-45a99263221b.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 76420-222-01 76420022201 2 VIAL, SINGLE-DOSE in 1 CARTON (76420-222-01) / 1 mL in 1 VIAL, SINGLE-DOSE 2009-06-01 0000-00-00 No No Current