Naloxone Hydrochloride 51662-1659-02
- Manufacturer
- Hf Acquisition Co Llc, Dba Healthfirst
- Dosage Form
- Spray
- Route
- Nasal
- Product Type
- Human Otc Drug
- Marketing Start
- July 30, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA211951
Active Ingredients
| Ingredient | Strength |
|---|---|
| Naloxone Hydrochloride | 4 mg/.1mL |
Drug Class
Opioid Antagonist [EPC]Opioid Antagonists [MoA]
Selected Package
51662-1659-02Selected2 VIAL, SINGLE-DOSE in 1 CARTON (51662-1659-2) / .1 mL in 1 VIAL, SINGLE-DOSE (51662-1659-1)