Naloxone Hydrochloride 70518-2725
Product NDC
70518-2725- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Injection
- Route
- Parenteral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 5, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA072076
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Naloxone Hydrochloride | 1 mg/mL |
Drug Class
Opioid Antagonist [EPC]Opioid Antagonists [MoA]
Packaging Options(1)
10 SYRINGE in 1 BOX (70518-2725-0) / 2 mL in 1 SYRINGE (70518-2725-1)