SOLU-CORTEF

Orange BookUNIISPLATC A07EA02

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

Identification

ManufacturerHF Acquisition Co. LLC, DBA HealthFirst

CountryUS (United States)

ATC codeA07EA02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
5166212611
2 mL in 1 VIAL, SINGLE-DOSE (51662-1261-1)
ndc11
5166212613
25 POUCH in 1 CASE (51662-1261-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1261-2) / 2 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": "51662-1261_1203ca7f-080b-4c49-e063-6294a90a90e0",
  "productndc": "51662-1261",
  "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": "SOLU-CORTEF",
  "start_marketing_date": "20180903",
  "active_numerator_strength": "100"
}

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