NDC 70069-835
Pemetrexed 500 mg per 20 mL injection, powder, lyophilized, for solution
On the label: Somerset Therapeutics, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Reliance Life Sciences Private Limited | Navi Mumbai, India | Makes it, makes the active ingredient, tests it, packages it and labels it | Serious problems, FDA actionFeb 27, 2026 · 8 inspections, 2 with FDA action |
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 ANDA211899
- On the market since
- Apr 15, 2025
- Package NDCs
70069-835-01- Official label
- DailyMed (National Library of Medicine), updated May 10, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?