triamcinolone acetonide

Generic: triamcinolone acetonide

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name triamcinolone acetonide
Generic Name triamcinolone acetonide
Labeler northstar rx llc
Dosage Form INJECTION, SUSPENSION
Routes
INTRA-ARTICULAR INTRAMUSCULAR
Active Ingredients

triamcinolone acetonide 200 mg/5mL

Manufacturer
NorthStar Rx LLC

Identifiers & Regulatory

Product NDC 16714-140
Product ID 16714-140_5838bced-e747-4fff-96a7-9eb89c82d785
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207550
Listing Expiration 2026-12-31
Marketing Start 2019-11-19

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 16714140
Hyphenated Format 16714-140

Supplemental Identifiers

RxCUI
1085754 1792144
UPC
0316714150017 0316714130255 0316714140018
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 ANDA207550 (source: ndc)
Routes
INTRA-ARTICULAR INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 200 mg/5mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (16714-140-01) / 5 mL in 1 VIAL
source: ndc

Packages (1)

16714-140-01 1 VIAL in 1 CARTON (16714-140-01) / 5 mL in 1 VIAL

Ingredients (1)

triamcinolone acetonide (200 mg/5mL)

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": "5838bced-e747-4fff-96a7-9eb89c82d785", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0316714150017", "0316714130255", "0316714140018"], "unii": ["F446C597KA"], "rxcui": ["1085754", "1792144"], "spl_set_id": ["5f3aaf3a-cc66-4d4f-b9b7-2c50c325d477"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (16714-140-01)  / 5 mL in 1 VIAL", "package_ndc": "16714-140-01", "marketing_start_date": "20191119"}], "brand_name": "Triamcinolone Acetonide", "product_id": "16714-140_5838bced-e747-4fff-96a7-9eb89c82d785", "dosage_form": "INJECTION, SUSPENSION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "16714-140", "generic_name": "Triamcinolone Acetonide", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Triamcinolone Acetonide", "active_ingredients": [{"name": "TRIAMCINOLONE ACETONIDE", "strength": "200 mg/5mL"}], "application_number": "ANDA207550", "marketing_category": "ANDA", "marketing_start_date": "20191119", "listing_expiration_date": "20261231"}