Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fenwal International, Inc. | Maricao, PR, United States | Makes it | Serious problems, FDA actionSep 24, 2021 · 8 inspections, 3 with FDA action |
Product details
- Generic drug
- Platelet Additive 3: every company that makes it
- Form
- solution, intravenous
- Strength
- 5 ingredients
- Approval
- NDA BN080041
- On the market since
- Jun 5, 2019
- Package NDCs
0942-9602-12- Official label
- DailyMed (National Library of Medicine), updated Oct 20, 2020
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