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United States · US · US:0009-0825_8512044a-4a54-4634-bb97-9e20126adc61
Solu-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
- ndc1100090825011 VIAL in 1 CARTON (0009-0825-01) / 2 mL in 1 VIAL
Annotations
UNII (FDA Substance ID)
50LQB69S1Z
HYDROCORTISONE SODIUM SUCCINATE
RxCUI 235483
Orange Book
N009866
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "50LQB69S1Z",
"rxcui": "235483",
"inchikey": "HHZQLQREDATOBM-CODXZCKSSA-M",
"display_name": "HYDROCORTISONE SODIUM SUCCINATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAMUSCULAR; INTRAVENOUS",
"spl_meta": {
"65eefd58-b166-4d71-ade6-45c8fdf86922": {
"match": "brand_token",
"title": "SOLU-CORTEF (HYDROCORTISONE SODIUM SUCCINATE) INJECTION, POWDER, FOR SOLUTION [PHARMACIA & UPJOHN COMPANY LLC]",
"spl_version": "29",
"published_date": "2025-09-10"
}
},
"productid": "0009-0825_8512044a-4a54-4634-bb97-9e20126adc61",
"productndc": "0009-0825",
"dosage_form": "INJECTION, POWDER, FOR SOLUTION",
"orange_book": {
"appl_no": "009866",
"products": [
{
"rs": true,
"rld": true,
"te_code": "AP",
"strength": "EQ 100MG BASE/VIAL",
"product_no": "001",
"approval_date": "Approved Prior to Jan 1, 1982"
},
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "EQ 250MG BASE/VIAL",
"product_no": "002",
"approval_date": "Approved Prior to Jan 1, 1982"
},
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "EQ 500MG BASE/VIAL",
"product_no": "003",
"approval_date": "Approved Prior to Jan 1, 1982"
},
{
"rs": true,
"rld": true,
"te_code": null,
"strength": "EQ 1GM BASE/VIAL",
"product_no": "004",
"approval_date": "Approved Prior to Jan 1, 1982"
}
],
"appl_type": "N"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "HYDROCORTISONE SODIUM SUCCINATE",
"proprietary_name": "Solu-Cortef",
"active_ingred_unit": "mg/2mL",
"application_number": "NDA009866",
"marketing_category": "NDA",
"nonproprietary_name": "hydrocortisone sodium succinate",
"start_marketing_date": "19550427",
"active_numerator_strength": "100"
}Related drugs
Other records sharing ATC code A07EA02.
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