Triamcinolone acetonide

Product NDC
53002-9770
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Triamcinolone acetonide
Dosage form
CREAM
Route
TOPICAL
Labeler
RPK Pharmaceuticals, Inc.
Application
ANDA088042
Marketing category
ANDA
Substance
TRIAMCINOLONE ACETONIDE
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
53002-9770-115 g in 1 TUBE (53002-9770-1) 2018-10-010000-00-00NoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
4ebb08c5-d822-46a0-8912-da6e79fc4a0aRPK Pharmaceuticals, Inc.2023-06-07Human Prescription Drug Label5