FDA.reportPublic FDA data

Triasil

Product NDC
59088-730
11-digit product format
590880730
Labeler code
59088
Product ID
59088-730_f3095546-7f72-2665-e053-2995a90aff07
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Triamcinolone Acetonide
Dosage form
KIT
Labeler
PureTek Corporation
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2023-01-20
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Triasil
Listing expiration
2026-12-31

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1085636Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
dcf6c630-6f5d-3d2f-e053-2995a90ad812Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d4d7da1a-7fd4-628e-cdae-89e749b1c534Product name720260127
75f7e47b-8736-a182-fc44-22aca8d79689Product name220251211
62986c8d-91f1-b1ba-b5a3-8b54b75bb8c2Product name620250516
e42f429b-c4e5-0402-e1c5-730154df4060Product name420240205
38d4de13-64b3-4057-b91c-4b5126962341Product name120220516
089e0644-1ea8-8654-4113-39f960dd57d5Product name320210115
1629e00f-54fb-4a43-8306-b58442b23902Product name920200430
5331c9c8-f64b-11e6-ccf1-071c477fcb0bProduct name720190612
9f64e0dc-109c-9660-8e0e-91ec987b3817Product name620171204
dfa879a3-32de-49f0-a7ba-9b9c3e13002fProduct name120171204
8de20f81-8411-4cf1-a8b2-03404ee56d01Product name320171109
a5f1a68c-0352-4f34-46a3-9b4eed239ed8Product name220160819
355b2224-0895-7135-83f5-d099a6a82a0aProduct name120140508
55be6b50-8cc0-f0f1-74a1-3416a91193aaProduct name120140508
7a0092d1-1e8c-0d78-4f8d-d95fa15cc3cfProduct name120140508
89b93c13-4be8-69f3-b33b-63e64feffb9bProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
45802-055-36Triasil1 in 1 CARTONOINTMENT1 mg in 1g2
45802-055-36Triasil80 g in 1 TUBEOINTMENT80 g1 mg in 1g2
59088-730-00Triasil1 in 1 KITKIT12

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59088-730-00EA - Each59088-730b53e98fb-7c23-41a8-b705-0e619f6942c512023-02-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59088-730TRIASIL (TRIAMCINOLONE ACETONIDE) KIT [PURETEK CORPORATION]2Current NDC, 3 package rows20230202_dcf6c630-6f5d-3d2f-e053-2995a90ad812.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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
TriasilTRIAMCINOLONE ACETONIDEPureTek Corporationdcf6c630-6f5d-3d2f-e053-2995a90ad8122023-01-24Adverse reactionsExact identifier
ndc (product): 59088-730

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1085636triamcinolone acetonide 0.1 % Topical OintmentPSNdcf6c630-6f5d-3d2f-e053-2995a90ad8122
1085636triamcinolone acetonide 0.001 MG/MG Topical OintmentSCDdcf6c630-6f5d-3d2f-e053-2995a90ad8122
1085636triamcinolone acetonide 0.1 % Topical OintmentSYdcf6c630-6f5d-3d2f-e053-2995a90ad8122

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
45802-055-36458020055361 in 1 CARTONHistorical
59088-730-00590880730001 KIT in 1 KIT (59088-730-00) * 1 TUBE in 1 CARTON (45802-055-36) / 80 g in 1 TUBE1 kit2023-01-20NoNoCurrent