NDC 63323-751
Phenylephrine Hydrochloride 10 mg per 1 mL injection
On the label: Fresenius Kabi, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Melrose Park, IL, United States | Makes it and tests it | Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action |
Product details
- Generic drug
- Phenylephrine: every company that makes it
- Form
- injection, intravenous
- Strength
- 10 mg per 1 mL
- Approval
- ANDA ANDA210666
- On the market since
- May 25, 2019
- Package NDCs
63323-751-0563323-751-10- Official label
- DailyMed (National Library of Medicine), updated Oct 20, 2026
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