Hydrocortisone sodium succinate
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Hydrocortisone sodium succinate
- Generic name
- HYDROCORTISONE SODIUM SUCCINATE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- d533ebee-9f1c-42d7-9808-ae5d5e55741b
- SPL ID
- 23cd0282-fb6b-4fb9-9b3a-0b23e8125625
- Version
- 1
- Effective date
- 2026-05-08
- Source export date
- 2026-09-28
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:15:10
| Harmonized routes |
|---|
| INTRAMUSCULAR, INTRAVENOUS |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | ANDA | 217191 | derived:openfda.application_number |
| application number | ANDA217191 | openfda.application_number | |
| brand name | Hydrocortisone sodium succinate | openfda.brand_name | |
| generic name | HYDROCORTISONE SODIUM SUCCINATE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 70771-1966-1 | openfda.package_ndc |
| ndc | product | 70771-1966 | openfda.product_ndc |
| ndc11 | package | 70771196601 | derived:openfda.package_ndc |
| rxcui | 238755 | openfda.rxcui | |
| spl id | 23cd0282-fb6b-4fb9-9b3a-0b23e8125625 | id | |
| spl set id | d533ebee-9f1c-42d7-9808-ae5d5e55741b | set_id | |
| unii | 50LQB69S1Z | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.