NDC 68083-412
Cangrelor 50 mg injection, powder, lyophilized, for solution
On the label: Gland Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Gland Pharma Limited | Hyderabad, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJul 25, 2024 · 7 inspections |
Product details
- Generic drug
- Cangrelor: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 50 mg
- Approval
- ANDA ANDA213551
- On the market since
- Aug 11, 2025
- Package NDCs
68083-412-10- Official label
- DailyMed (National Library of Medicine), updated Aug 14, 2025
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