NDC 36000-336
ephedrine sulfate 50 mg per 1 mL injection
On the label: Baxter Healthcare Corporation.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Baxter Pharmaceuticals India Private Limited | Ahmedabad, India | Makes it, tests it, packages it, labels it and sterilizes it | Serious problems, FDA actionJan 27, 2023 · 9 inspections, 3 with FDA action |
Product details
- Generic drug
- Ephedrine: every company that makes it
- Form
- injection, intravenous
- Strength
- 50 mg per 1 mL
- Approval
- ANDA ANDA216740
- On the market since
- Jul 8, 2026
- Package NDCs
36000-336-0136000-336-25- Official label
- DailyMed (National Library of Medicine), updated Jan 20, 2023
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