Naloxone Hydrochloride 00409-1782-69

Package NDC

00409-1782-69

Manufacturer: Hospira, Inc.
Dosage Form: Injection, Solution
Route: Intramuscular, Intravenous, And Subcutaneous
Product Type: Human Prescription Drug
Marketing Start: September 23, 2005
Listing Expires: December 31, 2026
Application: ANDA070172

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Active Ingredients

Ingredient	Strength
Naloxone Hydrochloride	.4 mg/mL

Drug Class

Opioid Antagonist [EPC]Opioid Antagonists [MoA]

Selected Package

00409-1782-69Selected

10 CARTRIDGE in 1 BOX (0409-1782-69) / 1 mL in 1 CARTRIDGE (0409-1782-03)