Naloxone Hydrochloride 76045-0114-10

Package NDC

76045-0114-10

Manufacturer: Fresenius Kabi Usa, Llc
Dosage Form: Injection, Solution
Route: Intramuscular, Intravenous, And Subcutaneous
Product Type: Human Prescription Drug
Marketing Start: April 2, 2024
Listing Expires: December 31, 2026
Application: ANDA213573

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Active Ingredients

Ingredient	Strength
Naloxone Hydrochloride	.4 mg/mL

Drug Class

Opioid Antagonist [EPC]Opioid Antagonists [MoA]

Selected Package

76045-0114-10Selected

24 SYRINGE in 1 CARTON (76045-114-10) / 1 mL in 1 SYRINGE (76045-114-01)