Naloxone Hydrochloride 70385-2033
Product NDC
70385-2033- Manufacturer
- Sina Health Inc
- Dosage Form
- Injection, Solution
- Route
- Intramuscular, Intravenous, And Subcutaneous
- Product Type
- Human Prescription Drug
- Marketing Start
- August 8, 2017
- Listing Expires
- December 31, 2027
- Application
- ANDA207633
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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 in 1 PACKAGE (70385-2033-1) / 1 mL in 1 VIAL