NDC 70710-1907
Hydrocortisone sodium succinate 100 mg per 2 mL injection
On the label: Zydus Pharmaceuticals (USA) Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Vadodara, India | Makes it and tests it | Serious problems, FDA actionApr 23, 2024 · 2 inspections, 1 with FDA action |
Recalls
- Oct 1, 2026 · Class II · Zydus Pharmaceuticals (USA) Inc
Failed Impurities/Degradation Specifications.
Lots: Lot #: LB00047A, LB00048A, Exp. Date 03/2028
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Hydrocortisone: every company that makes it
- Form
- injection, intramuscular; intravenous
- Strength
- 100 mg per 2 mL
- Approval
- ANDA ANDA217191
- On the market since
- May 9, 2026
- Package NDCs
70710-1907-1- Official label
- DailyMed (National Library of Medicine), updated May 8, 2026
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