NDC 70518-4433
Ephedrine Sulfate 50 mg per 1 mL injection
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Somerset Therapeutics, LLC's NDC 70069-819.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Gland Pharma Limited | Hyderabad, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJul 25, 2024 · 7 inspections |
Product details
- Generic drug
- Ephedrine: every company that makes it
- Form
- injection, intravenous
- Strength
- 50 mg per 1 mL
- Approval
- ANDA ANDA216146
- On the market since
- Aug 12, 2025
- Package NDCs
70518-4433-070518-4433-1- Official label
- DailyMed (National Library of Medicine), updated Sep 11, 2026
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