Naloxone Hydrochloride 76045-0112
Product NDC
76045-0112- Manufacturer
- Fresenius Kabi Usa, Llc
- Dosage Form
- Injection, Solution
- Route
- Intramuscular, Intravenous, And Subcutaneous
- Product Type
- Human Prescription Drug
- Marketing Start
- April 2, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA213573
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Naloxone Hydrochloride | 1 mg/mL |
Drug Class
Opioid Antagonist [EPC]Opioid Antagonists [MoA]
Packaging Options(1)
24 SYRINGE in 1 CASE (76045-112-20) / 2 mL in 1 SYRINGE (76045-112-01)