Naloxone Hydrochloride 70756-0658
Product NDC
70756-0658- Manufacturer
- Lifestar Pharma Llc
- Dosage Form
- Injection, Solution
- Route
- Intramuscular, Intravenous, And Subcutaneous
- Product Type
- Human Prescription Drug
- Marketing Start
- February 29, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA218404
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Naloxone Hydrochloride | .4 mg/mL |
Drug Class
Opioid Antagonist [EPC]Opioid Antagonists [MoA]
Packaging Options(3)
10 VIAL, SINGLE-DOSE in 1 CARTON (70756-658-10) / 1 mL in 1 VIAL, SINGLE-DOSE
25 VIAL, SINGLE-DOSE in 1 CARTON (70756-658-25) / 1 mL in 1 VIAL, SINGLE-DOSE
1 VIAL, SINGLE-DOSE in 1 CARTON (70756-658-82) / 1 mL in 1 VIAL, SINGLE-DOSE