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United States · US · US:70710-1907_9e47e808-7310-4c61-ac62-595a5c357123
Hydrocortisone sodium succinate
Orange BookUNIISPLATC A07EA02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerZydus Pharmaceuticals USA Inc.
CountryUS (United States)
ATC codeA07EA02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1170710190711 VIAL in 1 CARTON (70710-1907-1) / 2 mL in 1 VIAL
Annotations
UNII (FDA Substance ID)
50LQB69S1Z
HYDROCORTISONE SODIUM SUCCINATE
RxCUI 235483
Orange Book
A217191
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": {
"bc751403-94f2-4f9d-b533-cf6186a40ceb": {
"match": "brand_token",
"title": "HYDROCORTISONE TABLET [MYLAN PHARMACEUTICALS INC.]",
"spl_version": "12",
"published_date": "2026-05-27"
}
},
"productid": "70710-1907_9e47e808-7310-4c61-ac62-595a5c357123",
"productndc": "70710-1907",
"dosage_form": "INJECTION",
"orange_book": {
"appl_no": "217191",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "EQ 100MG BASE/VIAL",
"product_no": "001",
"approval_date": "May 7, 2026"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "HYDROCORTISONE SODIUM SUCCINATE",
"proprietary_name": "Hydrocortisone sodium succinate",
"active_ingred_unit": "mg/2mL",
"application_number": "ANDA217191",
"marketing_category": "ANDA",
"nonproprietary_name": "Hydrocortisone sodium succinate",
"start_marketing_date": "20260509",
"active_numerator_strength": "100"
}Related drugs
Other records sharing ATC code A07EA02.
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