Naloxone Hydrochloride 71872-7297
Product NDC
71872-7297- Manufacturer
- Medical Purchasing Solutions, Llc
- Dosage Form
- Injection, Solution
- Route
- Intramuscular, Intravenous, And Subcutaneous
- Product Type
- Human Prescription Drug
- Marketing Start
- January 29, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA214785
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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, SINGLE-DOSE in 1 BAG (71872-7297-1) / 1 mL in 1 VIAL, SINGLE-DOSE