NDC 68001-536
Pemetrexed 500 mg per 20 mL injection, powder, lyophilized, for solution
On the label: BluePoint Laboratories..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| EUGIA Pharma Specialities Limited | Medchal-Malkajgiri, India | Makes it and tests it | No problems foundJul 26, 2023 · 2 inspections |
Product details
- Generic drug
- Pemetrexed: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 500 mg per 20 mL
- Approval
- ANDA ANDA214632
- On the market since
- Jul 4, 2022
- Package NDCs
68001-536-41- Official label
- DailyMed (National Library of Medicine), updated Sep 5, 2023
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