Naloxone Hydrochloride 51662-1673-01

Package NDC

51662-1673-01

Manufacturer: Hf Acquisition Co. Llc. Dba Healthfirst
Dosage Form: Injection, Solution
Route: Intramuscular, Intravenous, And Subcutaneous
Product Type: Human Prescription Drug
Marketing Start: July 26, 2017
Listing Expires: December 31, 2027
Application: ANDA207634

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Active Ingredients

Ingredient	Strength
Naloxone Hydrochloride	.4 mg/mL

Drug Class

Opioid Antagonist [EPC]Opioid Antagonists [MoA]

Selected Package

51662-1673-01Selected

10 mL in 1 VIAL, GLASS (51662-1673-1)