Naloxone Hydrochloride 71872-7177-01

Package NDC

71872-7177-01

Manufacturer: Medical Purchasing Solutions, Llc
Dosage Form: Injection
Route: Parenteral
Product Type: Human Prescription Drug
Marketing Start: June 1, 2001
Listing Expires: December 31, 2026
Application: ANDA072076

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Active Ingredients

Ingredient	Strength
Naloxone Hydrochloride	1 mg/mL

Drug Class

Opioid Antagonist [EPC]Opioid Antagonists [MoA]

Selected Package

71872-7177-01Selected

1 SYRINGE in 1 BAG (71872-7177-1) / 2 mL in 1 SYRINGE