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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
- ndc1174157180601 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"strength": "0.025% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**",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"strength": "0.025% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**",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"
}Related drugs
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