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United States · US · US:70095-041_4583474c-40e7-dd9d-e063-6294a90a902a

Deflazacort

Orange BookUNIISPLATC H02AB13

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerSun Pharmaceutical Industries, Inc.
CountryUS (United States)
ATC codeH02AB13
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7009504130
    1 BOTTLE in 1 CARTON (70095-041-30) / 30 TABLET in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
KR5YZ6AE4B
DEFLAZACORT
RxCUI 22396
Orange Book
A217741
ABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "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": "70095-041_4583474c-40e7-dd9d-e063-6294a90a902a",
  "productndc": "70095-041",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "217741",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "6MG",
        "product_no": "001",
        "approval_date": "Mar 18, 2025"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "18MG",
        "product_no": "002",
        "approval_date": "Mar 18, 2025"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "30MG",
        "product_no": "003",
        "approval_date": "Mar 18, 2025"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "36MG",
        "product_no": "004",
        "approval_date": "Mar 18, 2025"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "DEFLAZACORT",
  "proprietary_name": "Deflazacort",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA217741",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Deflazacort",
  "start_marketing_date": "20250319",
  "active_numerator_strength": "18"
}

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