NDC 51662-1525
Succinylcholine Chloride 20 mg per 1 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Dr. Reddy's Laboratories Inc.'s NDC 43598-666.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| DR Reddy's Laboratories Limited | Srikakulam, India | Makes it and tests it | Problems found, fixed voluntarilyJul 18, 2025 · 1 inspection |
| Dr.reddy's Laboratories Limited | Visakhapatnam, India | Makes it and tests it | Problems found, fixed voluntarilyMay 17, 2024 · 9 inspections, 2 with FDA action |
| Gland Pharma Limited | Hyderabad, India | Makes it and tests it | Problems found, fixed voluntarilyJun 27, 2023 · 4 inspections |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Recalls
- Sep 26, 2025 · Class II · Dr. Reddy's Laboratories, Inc.
Out-of-Specification (OOS) result during the 6-month stability testing; decreased preservative concentration.
Lots: Lot # K250048
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 ANDA210698
- On the market since
- Jan 21, 2021
- Package NDCs
51662-1525-1- Official label
- DailyMed (National Library of Medicine), updated Jan 21, 2021
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