NDC 51662-1576
Phenylephrine Hydrochloride 10 mg per 1 mL injection
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Fresenius Kabi, LLC's NDC 63323-751.
Where the pills inside were 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 |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Phenylephrine: every company that makes it
- Form
- injection, intravenous
- Strength
- 10 mg per 1 mL
- Approval
- ANDA ANDA210665
- On the market since
- Jun 30, 2021
- Package NDCs
51662-1576-151662-1576-251662-1576-3- Official label
- DailyMed (National Library of Medicine), updated Feb 22, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?