triamcinolone acetonide

Generic: triamcinolone acetonide

Labeler: teva parenteral medicines, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name triamcinolone acetonide
Generic Name triamcinolone acetonide
Labeler teva parenteral medicines, inc.
Dosage Form INJECTION, SUSPENSION
Routes
INTRA-ARTICULAR INTRAMUSCULAR
Active Ingredients

triamcinolone acetonide 40 mg/mL

Manufacturer
Teva Parenteral Medicines, Inc.

Identifiers & Regulatory

Product NDC 0703-0241
Product ID 0703-0241_4d3cac2c-90fe-40a6-9a38-e0ae001fdfd3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209852
Marketing Start 2019-08-29
Marketing End 2026-12-31

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 07030241
Hyphenated Format 0703-0241

Supplemental Identifiers

RxCUI
1085754 1792144
UPC
0307030245013 0307030241015
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 ANDA209852 (source: ndc)
Routes
INTRA-ARTICULAR INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 40 mg/mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-0241-01) / 1 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

0703-0241-01 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-0241-01) / 1 mL in 1 VIAL, SINGLE-DOSE

Ingredients (1)

triamcinolone acetonide (40 mg/mL)

Linked Drug Pages (1)

Triamcinolone Acetonide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRA-ARTICULAR", "INTRAMUSCULAR"], "spl_id": "4d3cac2c-90fe-40a6-9a38-e0ae001fdfd3", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0307030245013", "0307030241015"], "unii": ["F446C597KA"], "rxcui": ["1085754", "1792144"], "spl_set_id": ["1680315d-dcdc-407a-b8e8-8710587197d2"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Teva Parenteral Medicines, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0703-0241-01)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0703-0241-01", "marketing_end_date": "20261231", "marketing_start_date": "20190829"}], "brand_name": "Triamcinolone Acetonide", "product_id": "0703-0241_4d3cac2c-90fe-40a6-9a38-e0ae001fdfd3", "dosage_form": "INJECTION, SUSPENSION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0703-0241", "generic_name": "Triamcinolone Acetonide", "labeler_name": "Teva Parenteral Medicines, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Triamcinolone Acetonide", "active_ingredients": [{"name": "TRIAMCINOLONE ACETONIDE", "strength": "40 mg/mL"}], "application_number": "ANDA209852", "marketing_category": "ANDA", "marketing_end_date": "20261231", "marketing_start_date": "20190829"}