Nalbuphine Hydrochloride 70069-0671-10

Package NDC

70069-0671-10

Manufacturer: Somerset Therapeutics, Llc
Dosage Form: Injection
Route: Intramuscular, Intravenous, And Subcutaneous
Product Type: Human Prescription Drug
Marketing Start: September 25, 2024
Listing Expires: December 31, 2026
Application: ANDA216050

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Active Ingredients

Ingredient	Strength
Nalbuphine Hydrochloride	10 mg/mL

Drug Class

Competitive Opioid Antagonists [MoA]Opioid Agonist/Antagonist [EPC]Partial Opioid Agonists [MoA]

Selected Package

70069-0671-10Selected

10 AMPULE in 1 CARTON (70069-671-10) / 1 mL in 1 AMPULE (70069-671-01)