NDC 69097-004
Hydrocortisone sodium succinate 100 mg per 2 mL injection
On the label: Cipla USA., Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Immacule Lifesciences Private Limited | Solan, India | Makes it, tests it, packages it and labels it | Serious problems, FDA actionSep 18, 2025 · 3 inspections, 1 with FDA action |
| Symbiotec Pharmalab Limited | Indore, India | Makes the active ingredient | Problems found, fixed voluntarilyApr 3, 2026 · 6 inspections |
Product details
- Generic drug
- Hydrocortisone: every company that makes it
- Form
- injection, intramuscular; intravenous
- Strength
- 100 mg per 2 mL
- Approval
- ANDA ANDA214050
- On the market since
- Sep 25, 2024
- Package NDCs
69097-004-67- Official label
- DailyMed (National Library of Medicine), updated Oct 29, 2026
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