Phenylephrine Hydrochloride 71839-0127-25

Package NDC

71839-0127-25

Manufacturer: Be Pharmaceuticals Inc.
Dosage Form: Injection
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: July 10, 2023
Listing Expires: December 31, 2026
Application: ANDA217521

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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

71839-0127-25Selected

25 VIAL, SINGLE-DOSE in 1 CARTON (71839-127-25) / 1 mL in 1 VIAL, SINGLE-DOSE (71839-127-01)