NDC 70710-1377
Succinylcholine Chloride 20 mg per 1 mL injection, solution
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
- Aug 27, 2025 · Class II · Zydus Pharmaceuticals (USA) Inc
Failed Impurities/Degradation Specifications: Out-of-Specification test results obtained for any individual unknown degradation impurity.
Lots: Lot #s: L400077, exp: 8/31/2025; L400113, exp.: 9/30/2025; L400372, L400373, exp.: 3/31/2026; L400374, exp.: 4/30/2026.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Succinylcholine: every company that makes it
- Form
- injection, solution, intramuscular; intravenous
- Strength
- 20 mg per 1 mL
- Approval
- ANDA ANDA209467
- On the market since
- May 10, 2018
- Package NDCs
70710-1377-170710-1377-2- Official label
- DailyMed (National Library of Medicine), updated Dec 23, 2022
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