Naloxone Hydrochloride 68001-0645
Product NDC
68001-0645- Manufacturer
- Bluepoint Laboratories
- Dosage Form
- Spray
- Route
- Nasal
- Product Type
- Human Otc Drug
- Marketing Start
- May 1, 2025
- Listing Expires
- December 31, 2027
- Application
- ANDA211951
Active Ingredients
| Ingredient | Strength |
|---|---|
| Naloxone Hydrochloride | 4 mg/.1mL |
Drug Class
Opioid Antagonist [EPC]Opioid Antagonists [MoA]
Packaging Options(1)
2 VIAL, SINGLE-DOSE in 1 CARTON (68001-645-45) / .1 mL in 1 VIAL, SINGLE-DOSE