Naloxone Hydrochloride 76329-1469-01

Package NDC

76329-1469-01

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]

Selected Package

76329-1469-01Selected

10 SYRINGE in 1 BOX (76329-1469-1) / 2 mL in 1 SYRINGE