NDC 0310-3200
Andexxa 200 mg per 20 mL injection, powder, lyophilized, for solution
On the label: AstraZeneca Pharmaceuticals LP.
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants AstraZeneca Pharmaceuticals LP names for other drugs.
Product details
- Generic drug
- Andexanet Alfa: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 200 mg per 20 mL
- Approval
- BLA BLA125586
- On the market since
- Jul 12, 2022
- Package NDCs
0310-3200-010310-3200-040310-3200-05- Official label
- DailyMed (National Library of Medicine), updated May 23, 2025
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