NDC 0641-6150
Neostigmine Methylsulfate 0.5 mg per 1 mL injection
On the label: Hikma Pharmaceuticals USA Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hikma Pharmaceuticals USA Inc. | Cherry Hill, NJ, United States | Makes it, tests it, packages it and labels it | No problems foundMay 13, 2026 · 18 inspections |
Product details
- Generic drug
- Neostigmine: every company that makes it
- Form
- injection, intravenous
- Strength
- 0.5 mg per 1 mL
- Approval
- ANDA ANDA207042
- On the market since
- Dec 28, 2015
- Package NDCs
0641-6150-010641-6150-100641-6150-25- Official label
- DailyMed (National Library of Medicine), updated Mar 18, 2026
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