triamcinolone acetonide

Generic: triamcinolone acetonide

Labeler: e. fougera & co. a division of fougera pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name triamcinolone acetonide
Generic Name triamcinolone acetonide
Labeler e. fougera & co. a division of fougera pharmaceuticals, llc
Dosage Form OINTMENT
Routes
TOPICAL
Active Ingredients

triamcinolone acetonide .25 mg/g

Manufacturer
E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 0168-0005
Product ID 0168-0005_4ecf8bca-6585-4eed-88c7-c261a622d1cd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA085691
Listing Expiration 2027-12-31
Marketing Start 1978-02-14

Pharmacologic Class

Established (EPC)
corticosteroid [epc]
Mechanism of Action
corticosteroid hormone receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01680005
Hyphenated Format 0168-0005

Supplemental Identifiers

RxCUI
1085633 1085636
UPC
0301680006154
UNII
F446C597KA
NUI
N0000175576 N0000175450

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name triamcinolone acetonide (source: ndc)
Generic Name triamcinolone acetonide (source: ndc)
Application Number ANDA085691 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .25 mg/g
source: ndc
Packaging
  • 80 g in 1 TUBE (0168-0005-80)
source: ndc

Packages (1)

0168-0005-80 80 g in 1 TUBE (0168-0005-80)

Ingredients (1)

triamcinolone acetonide (.25 mg/g)

Linked Drug Pages (1)

Triamcinolone Acetonide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4ecf8bca-6585-4eed-88c7-c261a622d1cd", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0301680006154"], "unii": ["F446C597KA"], "rxcui": ["1085633", "1085636"], "spl_set_id": ["a5cc640f-c72d-49fa-b970-906c9ffd8629"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 g in 1 TUBE (0168-0005-80)", "package_ndc": "0168-0005-80", "marketing_start_date": "19780214"}], "brand_name": "Triamcinolone Acetonide", "product_id": "0168-0005_4ecf8bca-6585-4eed-88c7-c261a622d1cd", "dosage_form": "OINTMENT", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0168-0005", "generic_name": "triamcinolone acetonide", "labeler_name": "E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Triamcinolone Acetonide", "active_ingredients": [{"name": "TRIAMCINOLONE ACETONIDE", "strength": ".25 mg/g"}], "application_number": "ANDA085691", "marketing_category": "ANDA", "marketing_start_date": "19780214", "listing_expiration_date": "20271231"}