United States· US:59651-601_dc2886e0-4e19-4a7c-b7ae-5723d7b4b8c9

Deflazacort

A deflazacort product containing deflazacort, registered in United States by Aurobindo Pharma Limited. The same ATC class is registered in 8 of our 19 countries.

ATC H02AB13Orange BookUS label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normalisedDeflazacortATCH02AB13REGISTER NO.US:59651-601_dc2886e0…PACKS LISTED1CHECKEDJune 3, 2026

Where it is registered

Deflazacort is registered in 8 of 19 countries.

Countries holding a registration under ATC H02AB13 (deflazacort), each read from that country’s own register.

  • This record: United States, from FDA National Drug Code directory (United States)
  • 3 of them publish a price we can compare per daily dose

Deflazacort · ATC H02AB13

8 / 19 countries

  • Denmark
  • Finlandprice
  • Germany
  • Netherlands
  • Norwayprice
  • Sweden
  • United Kingdom
  • United Statesprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

Price per daily dose

What a daily dose of deflazacort costs, country by country.

Normalised to the WHO defined daily dose (15 mg), so markets compare like for like.

  • 1 market with a comparable price for this class
  • Public list prices, converted to USD at the rate date shown

Deflazacort · price per daily dose (15 mg)

USD · FX 28 Sept 2026

  • ES Spain$0.19
Median listed price per WHO defined daily dose, in each market that publishes a price. Open the full comparison

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
Deflazacort
Manufacturer
Aurobindo Pharma Limited
Country
United States (US)
ATC code
H02AB13
ATC class
Deflazacort
Defined daily dose
15 mg, O
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
June 3, 2026

Packs & prices · 1

  • ndc11
    5965160130
    30 TABLET in 1 BOTTLE (59651-601-30)

Regulatory notes

UNII (FDA substance ID)
KR5YZ6AE4B
DEFLAZACORT
RxCUI 22396
Orange Book
A217123
ABABABAB
DailyMed SPL labels
1 version tracked

Interactions

434 interactions on record for deflazacort.

Graded by severity as the source publishes them — 129 severe. Severity grades are free for everyone; mechanism and management come with Growth.

  • Severity for every pair — free, no plan needed
  • The source, licence and sync date on every record
  • Mechanism and what to do for each pair — Growth plan

Deflazacort · interactions on record

434 records

  • 129 severe
  • 297 moderate
  • 8 minor

Most severe, free to view

  • AprepitantA04AD12severe
  • LonafarnibA16AX20severe
  • DesirudinB01AE01severe
  • BerotralstatB06AC06severe
  • Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

Same medicine, other countries

Deflazacort in 7 other countries

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

All deflazacort products

Authorised across Europe · EMA

The same active substance is authorised in 10 EEA countries. Names it is sold under:

  • Germany · Calcort, Deflazacort Galen
  • Denmark · Deflazacort Vital Pharma Nordic
  • Spain · Defal, Deflazacort Cinfa
  • Finland · Deflazacort Vital Pharma Nordic
  • United Kingdom (Northern Ireland) · Calcort
  • Italy · Decor, Deflan
  • Netherlands · Deflazacort Xgx Pharma
  • Norway · Deflazacort Xgx Pharma
  • Portugal · Deflazacorte Acizan, Deflazacorte Almus
  • Sweden · Deflazacort

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/d9b39b76-bcfe-4bd3-8c77-6b0b79335102
GET /v1/drugs/d9b39b76-bcfe-4bd3-8c77-6b0b79335102?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.

{
  "unii": {
    "unii": "KR5YZ6AE4B",
    "rxcui": "22396",
    "inchikey": "FBHSPRKOSMHSIF-GRMWVWQJSA-N",
    "display_name": "DEFLAZACORT",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "2fac1332-0247-1047-e063-6294a90a557f": {
      "match": "brand_token",
      "title": "DEFLAZACORT ORAL SUSPENSION (DEFLAZACORT ORAL) SUSPENSION [SUN PHARMACEUTICAL INDUSTRIES, INC.]",
      "spl_version": "2",
      "published_date": "2026-02-02"
    }
  },
  "productid": "59651-601_dc2886e0-4e19-4a7c-b7ae-5723d7b4b8c9",
  "productndc": "59651-601",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "217123",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "6MG",
        "product_no": "001",
        "approval_date": "Feb 9, 2024"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "18MG",
        "product_no": "002",
        "approval_date": "Feb 9, 2024"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "30MG",
        "product_no": "003",
        "approval_date": "Feb 9, 2024"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "36MG",
        "product_no": "004",
        "approval_date": "Feb 9, 2024"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "DEFLAZACORT",
  "proprietary_name": "Deflazacort",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA217123",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Deflazacort",
  "start_marketing_date": "20240209",
  "active_numerator_strength": "30"
}

See everything about deflazacort.

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.