NDC 51662-1620
NALOXONE HCl 4 mg per 0.1 mL spray
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged from NDC 45802-811, made by Padagis Israel Pharmaceuticals Ltd (Naloxone Hydrochloride). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that relabels it). 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 HF Acquisition Co. LLC. DBA HealthFirst names for other drugs.
Product details
- Generic drug
- Naloxone: every company that makes it
- Form
- spray, nasal
- Strength
- 4 mg per 0.1 mL
- Approval
- ANDA ANDA211951
- On the market since
- Apr 10, 2023
- Package NDCs
51662-1620-151662-1620-2- Official label
- DailyMed (National Library of Medicine), updated Jan 28, 2024
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