NDC 72338-101
Pemetrexed 500 mg per 20 mL injection, powder, lyophilized, for solution
On the label: Waverley Pharma Inc.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Reliance Life Sciences Private Limited | Navi Mumbai, India | Makes it, makes the active ingredient and packages 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
- Jun 4, 2018
- Package NDCs
72338-101-01- Official label
- DailyMed (National Library of Medicine), updated Dec 30, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?