NDC 51662-1240
Narcan Naloxone Hci 4 mg per 0.1 mL spray
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Emergent Devices Inc.'s NDC 69547-353.
Where the pills inside were 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 Emergent Devices Inc. names for other drugs.
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Recalls
- Mar 15, 2021 · Class II · Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: 201701
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Naloxone: every company that makes it
- Form
- spray, nasal
- Strength
- 4 mg per 0.1 mL
- Approval
- NDA NDA208411
- On the market since
- Oct 15, 2018
- Package NDCs
51662-1240-151662-1240-2- Official label
- DailyMed (National Library of Medicine), updated Oct 10, 2023
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