Solu-Cortef

Orange BookUNIISPLATC A07EA02

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

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

ndc11
0009001612
1 VIAL, SINGLE-DOSE in 1 CARTON (0009-0016-12) / 4 mL in 1 VIAL, SINGLE-DOSE

Annotations

UNII (FDA Substance ID)

50LQB69S1Z

HYDROCORTISONE SODIUM SUCCINATE

RxCUI 235483

Orange Book

N009866

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": "0009-0016_8512044a-4a54-4634-bb97-9e20126adc61",
  "productndc": "0009-0016",
  "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/4mL",
  "application_number": "NDA009866",
  "marketing_category": "NDA",
  "nonproprietary_name": "hydrocortisone sodium succinate",
  "start_marketing_date": "19550427",
  "active_numerator_strength": "500"
}

Related drugs

Other records sharing ATC code A07EA02.

Access this data programmatically

Query Solu-Cortef and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.

Get a free API key Read the API docs