Phenylephrine Hydrochloride 70069-0801-25

Package NDC

70069-0801-25

Manufacturer: Somerset Therapeutics, Llc
Dosage Form: Injection
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: September 22, 2021
Listing Expires: December 31, 2026
Application: ANDA213318

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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

70069-0801-25Selected

25 VIAL in 1 CARTON (70069-801-25) / 1 mL in 1 VIAL (70069-801-01)