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United States · US · US:74157-180_39d4fc80-5bee-3f1d-e063-6294a90a3d69

CORDRAN

Orange BookUNIISPLATC D07AC07

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

Identification

ManufacturerINA Pharmaceutics, Inc
CountryUS (United States)
ATC codeD07AC07
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7415718060
    1 TUBE in 1 CARTON (74157-180-60) / 60 g in 1 TUBE

Annotations

UNII (FDA Substance ID)
8EUL29XUQT
FLURANDRENOLIDE
RxCUI 4500
Orange Book
N012806
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "8EUL29XUQT",
    "rxcui": "4500",
    "inchikey": "POPFMWWJOGLOIF-XWCQMRHXSA-N",
    "display_name": "FLURANDRENOLIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "39c0d1e6-6816-7ae5-e063-6394a90a592e": {
      "match": "brand_token",
      "title": "CORDRAN (FLURANDRENOLIDE) CREAM [INA PHARMACEUTICS, INC]",
      "spl_version": "2",
      "published_date": "2025-07-15"
    }
  },
  "productid": "74157-180_39d4fc80-5bee-3f1d-e063-6294a90a3d69",
  "productndc": "74157-180",
  "dosage_form": "CREAM",
  "orange_book": {
    "appl_no": "012806",
    "products": [
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "0.05%",
        "product_no": "001",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "0.05%",
        "product_no": "002",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "0.025% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**",
        "product_no": "003",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "0.025% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**",
        "product_no": "004",
        "approval_date": "Approved Prior to Jan 1, 1982"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "FLURANDRENOLIDE",
  "proprietary_name": "CORDRAN",
  "active_ingred_unit": "mg/g",
  "application_number": "NDA012806",
  "marketing_category": "NDA",
  "nonproprietary_name": "Flurandrenolide",
  "start_marketing_date": "20250707",
  "active_numerator_strength": ".5"
}

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