Naloxone Hydrochloride 00409-1219-01

Package NDC

00409-1219-01

Manufacturer: Hospira, Inc.
Dosage Form: Injection, Solution
Route: Intramuscular, Intravenous, And Subcutaneous
Product Type: Human Prescription Drug
Marketing Start: September 2, 2005
Listing Expires: December 31, 2027
Application: ANDA070257

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Active Ingredients

Ingredient	Strength
Naloxone Hydrochloride	.4 mg/mL

Drug Class

Opioid Antagonist [EPC]Opioid Antagonists [MoA]

Selected Package

00409-1219-01Selected

25 CARTON in 1 CASE (0409-1219-01) / 1 VIAL, MULTI-DOSE in 1 CARTON / 10 mL in 1 VIAL, MULTI-DOSE (0409-1219-41)