Naloxone Hcl 51662-1620
Product NDC
51662-1620- Manufacturer
- Hf Acquisition Co Llc, Dba Healthfirst
- Dosage Form
- Spray
- Route
- Nasal
- Product Type
- Human Prescription Drug
- Marketing Start
- April 10, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA211951
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Naloxone Hydrochloride | 4 mg/.1mL |
Drug Class
Opioid Antagonist [EPC]Opioid Antagonists [MoA]
Packaging Options(2)
.1 mL in 1 VIAL, SINGLE-DOSE (51662-1620-1)
2 VIAL, SINGLE-DOSE in 1 CARTON (51662-1620-2) / .1 mL in 1 VIAL, SINGLE-DOSE