Naloxone Hydrochloride 51662-1671
Product NDC
51662-1671- Manufacturer
- Hf Acquisition Co Llc, Dba Healthfirst
- Dosage Form
- Injection
- Route
- Intramuscular, Intravenous, And Subcutaneous
- Product Type
- Human Prescription Drug
- Marketing Start
- September 24, 1986
- Listing Expires
- December 31, 2026
- Application
- ANDA070299
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Naloxone Hydrochloride | .4 mg/mL |
Drug Class
Opioid Antagonist [EPC]Opioid Antagonists [MoA]
Packaging Options(1)
25 VIAL in 1 CARTON (51662-1671-3) / 1 mL in 1 VIAL (51662-1671-1)