Phenylephrine Hydrochloride 65219-0388-01

Package NDC

65219-0388-01

Manufacturer: Fresenius Kabi Usa, Llc
Dosage Form: Injection
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: May 10, 2026
Listing Expires: December 31, 2026
Application: ANDA210665

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Active Ingredients

Ingredient	Strength
Phenylephrine Hydrochloride	10 mg/mL

Drug Class

Adrenergic alpha1-Agonists [MoA]alpha-1 Adrenergic Agonist [EPC]

Selected Package

65219-0388-01Selected

25 VIAL, SINGLE-DOSE in 1 CARTON (65219-388-01) / 1 mL in 1 VIAL, SINGLE-DOSE (65219-388-00)