Naloxone Hydrochloride 51662-1586
Product NDC
51662-1586- Manufacturer
- Hf Acquisition Co Llc, Dba Healthfirst
- Dosage Form
- Injection, Solution
- Route
- Intramuscular, Intravenous, And Subcutaneous
- Product Type
- Human Prescription Drug
- Marketing Start
- August 16, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA213279
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Naloxone Hydrochloride | 1 mg/mL |
Drug Class
Opioid Antagonist [EPC]Opioid Antagonists [MoA]
Packaging Options(2)
1 SYRINGE in 1 BOX (51662-1586-1) / 2 mL in 1 SYRINGE
10 POUCH in 1 CASE (51662-1586-3) / 1 BOX in 1 POUCH (51662-1586-2) / 1 SYRINGE in 1 BOX / 2 mL in 1 SYRINGE