NDCFind

Naloxone Hydrochloride 51662-1671-03

Package NDC

51662-1671-03

Product NDC: 51662-1671

Manufacturer
Hf Acquisition Co Llc, Dba Healthfirst
Dosage Form
Injection
Route
Intramuscular, Intravenous, And Subcutaneous
Product Type
Human Prescription Drug
Marketing Start
September 24, 1986
Listing Expires
December 31, 2026
Application
ANDA070299
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Active Ingredients

IngredientStrength
Naloxone Hydrochloride.4 mg/mL

Drug Class

Opioid Antagonist [EPC]Opioid Antagonists [MoA]

Selected Package

51662-1671-03Selected

25 VIAL in 1 CARTON (51662-1671-3) / 1 mL in 1 VIAL (51662-1671-1)