Naloxone Hydrochloride 51662-1426
Product NDC
51662-1426- Manufacturer
- Hf Acquisition Co Llc, Dba Healthfirst
- Dosage Form
- Injection, Solution
- Route
- Intramuscular, Intravenous, And Subcutaneous
- Product Type
- Human Prescription Drug
- Marketing Start
- January 10, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA207634
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Naloxone Hydrochloride | .4 mg/mL |
Drug Class
Opioid Antagonist [EPC]Opioid Antagonists [MoA]
Packaging Options(1)
1 VIAL, GLASS in 1 CARTON (51662-1426-1) / 10 mL in 1 VIAL, GLASS