Naloxone Hydrochloride 70069-0071-10

Package NDC

70069-0071-10

Manufacturer: Somerset Therapeutics, Llc
Dosage Form: Injection, Solution
Route: Intramuscular, Intravenous, And Subcutaneous
Product Type: Human Prescription Drug
Marketing Start: August 8, 2017
Listing Expires: December 31, 2027
Application: ANDA207633

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Active Ingredients

Ingredient	Strength
Naloxone Hydrochloride	.4 mg/mL

Drug Class

Opioid Antagonist [EPC]Opioid Antagonists [MoA]

Selected Package

70069-0071-10Selected

10 VIAL in 1 CARTON (70069-071-10) / 1 mL in 1 VIAL (70069-071-01)