Naloxone Hydrochloride 00404-9922
Product NDC
00404-9922- Manufacturer
- Henry Schein, Inc
- Dosage Form
- Injection
- Route
- Parenteral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 13, 2022
- 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)
1 SYRINGE in 1 BAG (0404-9922-02) / 2 mL in 1 SYRINGE