Naloxone Hydrochloride 76329-1469
Product NDC
76329-1469- Manufacturer
- International Medication Systems, Limited
- Dosage Form
- Injection
- Route
- Parenteral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 1, 1988
- Listing Expires
- December 31, 2026
- 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)
10 SYRINGE in 1 BOX (76329-1469-1) / 2 mL in 1 SYRINGE