United States· US:70121-1655_34fc1ca6-3e1a-443a-9d5a-ef43b953df12

Triamcinolone Acetonide

A medicinal product containing triamcinolone acetonide, registered in United States by Amneal Pharmaceuticals LLC.

Checked against FDA National Drug Code directory (United States) on September 27, 2026

Informational only — not a medical device.

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The record

At a glance

FDA National Drug Code directory (United States)

Active substance: TRIAMCINOLONE ACETONIDE
Manufacturer: Amneal Pharmaceuticals LLC
Country: United States (US)
ATC code: —
Reimbursed: Not published by this register
Source register: FDA National Drug Code directory (United States)
Last checked: September 27, 2026

Packs & prices · 1

ndc11
70121-1655-1

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Same medicine, other countries

Triamcinolone acetonide in 16 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All triamcinolone acetonide products

Authorised across Europe · EMA

The same active substance is authorised in 28 EEA countries. Names it is sold under:

Austria · Volon, Volon A
Belgium · Delphi, Kenacort-A
Cyprus · Triacort
Czechia · Triamcinolon Léčiva
Germany · Nasacort, Rhinisan
Denmark · Kenalog, Triamcinolone Acetonide Medipha
Estonia · Kenalog
Spain · Nasacort
Finland · Nasacort, Triamcinolone Medipha
France · Kenacort Retard, Nasacort
United Kingdom (Northern Ireland) · Nasacort
Greece · Jiven, Nasacort
Croatia · Kenalog
Hungary · Ftorocort, Kenalog
Ireland · Nasacort, Nasacort Allergy
Iceland · Kenacort-T, Nasacort
Italy · Kenacort, Nasacort
Lithuania · Ftorocort, Kenalog
Luxembourg · Delphi, Kenacort-A
Latvia · Ftorocort, Kenalog
Malta · Nasacort, Nasacort Allergy
Netherlands · Cremor Triamcinolonacetonide, Kenacort-A 10
Norway · Kenacort-T, Nasacort
Poland · Polcortolon
Portugal · Nasacort, Telfast Spray Nasal
Sweden · Kenacort-T, Nasacort
Slovenia · Kenalog
Slovakia · Triamcinolon Crm Léčiva, Triamcinolon Ung Léčiva

Source: European Medicines Agency, Article 57 product data.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload

GET /v1/drugs/f1befb2d-7b8b-4dc5-af60-7a5d25e3c0f2
GET /v1/drugs/f1befb2d-7b8b-4dc5-af60-7a5d25e3c0f2?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "INTRA-ARTICULAR; INTRAMUSCULAR",
  "source": "ndc",
  "strength": "400",
  "substance": "TRIAMCINOLONE ACETONIDE",
  "productndc": "70121-1655",
  "dosage_form": "INJECTION, SUSPENSION",
  "dea_schedule": null,
  "strength_unit": "mg/10mL",
  "application_number": "ANDA207550",
  "marketing_category": "ANDA"
}

API reference MCP server Plans

See everything about triamcinolone acetonide.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.

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