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United States · US · US:0009-0031_17306ca2-c631-4281-824c-1cb6d63dcac1
CORTEF
Orange BookUNIISPLATC A07EA02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPharmacia & Upjohn Company LLC
CountryUS (United States)
ATC codeA07EA02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc110009003101100 TABLET in 1 BOTTLE (0009-0031-01)
Annotations
UNII (FDA Substance ID)
WI4X0X7BPJ
HYDROCORTISONE
RxCUI 5492
Orange Book
N008697
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "WI4X0X7BPJ",
"rxcui": "5492",
"inchikey": "JYGXADMDTFJGBT-VWUMJDOOSA-N",
"display_name": "HYDROCORTISONE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"9ce19944-dd88-4a7b-84ca-b07f4ec23bad": {
"match": "brand_token",
"title": "CORTEF (HYDROCORTISONE) TABLET [PHARMACIA & UPJOHN COMPANY LLC]",
"spl_version": "17",
"published_date": "2025-02-21"
}
},
"productid": "0009-0031_17306ca2-c631-4281-824c-1cb6d63dcac1",
"productndc": "0009-0031",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "008697",
"products": [
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "10MG",
"product_no": "001",
"approval_date": "Approved Prior to Jan 1, 1982"
},
{
"rs": true,
"rld": true,
"te_code": "AB",
"strength": "20MG",
"product_no": "002",
"approval_date": "Approved Prior to Jan 1, 1982"
},
{
"rs": false,
"rld": true,
"te_code": "AB",
"strength": "5MG",
"product_no": "003",
"approval_date": "Approved Prior to Jan 1, 1982"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "HYDROCORTISONE",
"proprietary_name": "CORTEF",
"active_ingred_unit": "mg/1",
"application_number": "NDA008697",
"marketing_category": "NDA",
"nonproprietary_name": "hydrocortisone",
"start_marketing_date": "19521215",
"active_numerator_strength": "10"
}Related drugs
Other records sharing ATC code A07EA02.
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