Naloxone Hydrochloride 51662-1239-03

Package NDC

51662-1239-03

Manufacturer: Hf Acquisition Co. Llc, Dba Healthfirst
Dosage Form: Injection
Route: Parenteral
Product Type: Human Prescription Drug
Marketing Start: September 3, 2018
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

51662-1239-03Selected

10 POUCH in 1 CASE (51662-1239-3) / 1 mL in 1 POUCH (51662-1239-2)

Other packages for this product(1)

51662-1239-01

1 SYRINGE, PLASTIC in 1 BOX (51662-1239-1) / 2 mL in 1 SYRINGE, PLASTIC

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