Naloxone Hydrochloride 72603-0590
Product NDC
72603-0590- Manufacturer
- Northstar Rxllc
- Dosage Form
- Injection, Solution
- Route
- Intramuscular, Intravenous, And Subcutaneous
- Product Type
- Human Prescription Drug
- Marketing Start
- July 1, 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(2)
10 VIAL, SINGLE-DOSE in 1 CARTON (72603-590-10) / 1 mL in 1 VIAL, SINGLE-DOSE (72603-590-01)
25 VIAL, SINGLE-DOSE in 1 CARTON (72603-590-25) / 1 mL in 1 VIAL, SINGLE-DOSE (72603-590-01)